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Hemoglobin
international journal for hemoglobin research
Volume 6, 1982 - Issue 1
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Original Article

Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin Genes

M. Poncz Division of Hematology The Children's Hospital of Philadelphia Departments of Pediatrics and Human Genetics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, 19104
,
D. Solowiejczyk Division of Hematology The Children's Hospital of Philadelphia Departments of Pediatrics and Human Genetics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, 19104
,
B. Harpel Division of Hematology The Children's Hospital of Philadelphia Departments of Pediatrics and Human Genetics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, 19104
,
Y. Mory The Weizmann Institute of Science, Rehovot, Israel
,
E. Schwartz Division of Hematology The Children's Hospital of Philadelphia Departments of Pediatrics and Human Genetics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, 19104
&
S. Surrey Division of Hematology The Children's Hospital of Philadelphia Departments of Pediatrics and Human Genetics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, 19104
Pages 27-36 | Received 05 Aug 1981, Accepted 25 Oct 1981, Published online: 07 Jul 2009

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L. Pagano, S. Desicato, A. Viola, C. De Rosa & G. Fioretti. (1995) Identification of the -92 (C→T) Mutation by the Amplification Refractory Mutation Sym in Southern Italy. Hemoglobin 19:5, pages 307-310.
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J. G. Hendy & M. N. Cauchi. (1994) Hb I-toulouse [β66(E10)LYS→GLU] in association with α-thalassemia. Hemoglobin 18:3, pages 227-229.
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E. Baysal, S. Sharma, S. C. Wong, V. B. Jogessar & T. H.J. Huisman. (1994) Distribution of β-thalassemia mutations in three asian indian populations with distant geographical locations. Hemoglobin 18:3, pages 201-209.
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W-D. Chen, P-C. Jia, S-S. Chen, C-C. Liang, B-S. Wang, S. Gao, X-J. Wang, M. Wang & S-K. Qu. (1994) The Gγ:Aγ ratios in the fetal hemoglobin of newborns of the man ethnic group and their γ-globin gene arrangements. Hemoglobin 18:3, pages 193-199.
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D. D. Pobedimskaya, T. P. Molchanova & T. H. J. Huisman. (1994) Hb Ramona or α224(B5)TYR->CYSβ2. Hemoglobin 18:4-5, pages 365-366.
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L. Jankovic, D. Plaseska, G. D. Efremov, P. Tchaicarova & G. H. Petkov. (1994) Two Rare Mutations [CD 30 (G->C) and CDs 36/37 (−T)] in a Turkish Thalassemia Major Patient from Bulgaria. Hemoglobin 18:4-5, pages 359-364.
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W-B Qin, X-L Yue, L-Y Qin, T-L Jü, J. B. Wilson, L-H. Gu & T. H. J. Huisman. (1994) Two Rare Hemoglobin Variants: Hb Pyrgos [β83(ef7)Gly->Asp] and Hb Legnano [α141(hc3)arg->leu] Found in Inner Mongolia, P.R. China. Hemoglobin 18:4-5, pages 343-345.
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M. F. G. Sadiq & T. H. J. Huisman. (1994) Molecular Characterization of β-Thalassemia in North Jordan. Hemoglobin 18:4-5, pages 325-332.
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W-B. Qin, D. D. Pobedimskaya, T. P. Molchanova, J. B. Wilson, L-H Gu, J.M de Pablos & T. H. J. Huisman. (1994) Hb Fannin-Lubbock in Five Spanish Families is Characterized by two Mutations: β111 GTC->CTC (VAL->LEU) AND β119 GGC->GAC (GLY->ASP). Hemoglobin 18:4-5, pages 297-306.
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N. H. Jiang, S. Liang, C. Su, J. F. Nechtman & T. A. Stoming. (1993) A Novel β-Thalassemia Mutation [IVS-II-5 (G→C)] in a Chinese Family from Guangxi Province, P. R. China. Hemoglobin 17:6, pages 563-567.
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D. D. Pobedimskaya, T. P. Molchanova, T. H. J. Huisman, S. R. Harding & R. Bakanec. (1993) HB F-Saskatoon or α2Gγ221(B3)GLU→LYS Observed in a North American Indian Newborn. Hemoglobin 17:6, pages 547-549.
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H-J. Li, W-Z. Yu, C-H. Zhou, X-J. Hao & Y. Zhou. (1993) The β-Thalassemia Frameshift at Codon 8 (-AA) Observed in four Chinese of the Uygur Nationality. Hemoglobin 17:6, pages 537-541.
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D. D. Pobedimskaya, T. P. Molchanova, R. Amernick, M. S. Druskin, B. B. Webber, J. B. Wilson & T. H. J. Huisman. (1993) HB Sinai-Baltimore or α2β218(A15)VAL→GLY, a Silent, Mildly Unstable β Chain Variant Detected by Isoelectrofocusing and High Performance Liquid Chromatography. Hemoglobin 17:6, pages 505-512.
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T. P. Molchanova, Y. V. Postnikov, L-H. Gu & T. H. J. Huisman. (1993) HB A2−Grovetown or α2δ275(El9)Leu→val. Hemoglobin 17:3, pages 289-291.
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D. D. Pobedimskaya, T. P. Molchanova, L-H. Gu, M. A. Molina, J. M. De Pablos & T. H. J. Huisman. (1993) HB F-Sacromonte or α2Gγ259(E3)LYS→GLN Observed in a Spanish Newborn and His Mother. Hemoglobin 17:3, pages 269-274.
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T. P. Molchanova, Yu. V. Postnikov, J. F. Prior, J. L. Raven & J. A. Bennett. (1993) HB Tigraye OR α2β279(EF3)ASP→HIS(GAC→CAC): A Hemoglobin Variant with Increased Oxygen Affinity Observed in an Ethiopian Male. Hemoglobin 17:3, pages 247-250.
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T. P. Molchanova, Yu. V. Postnikov, D. D. Pobedimskaya, N. S. Smetanina, A. A. Moschan, E. G. Kazanetz, Yu. N. Tokarev & T. H. J. Huisman. (1993) HB Alesha or α2 β267(E11)VAL →MET: A New Unstable Hemoglobin Variant Identified Through Sequencing of, Amplified DNA. Hemoglobin 17:3, pages 217-225.
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D. Plaseska, S. Koceva, N. Rasovic & G. D. Efremov. (1993) HB Volga [β27(B9)ALA→ASP]: Detection of a DE Novo Mutation by AVA II Digestion of PCR-Amplified DNA. Hemoglobin 17:3, pages 209-215.
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F. Kutlar, A. Kutlar, E. Nuguid, J. Prchal & T. H. J. Huisman. (1993) Usefulness of HPLC Methodology for the Characterization of Combinations of the Common β Chain Variants HBS S, C, and O-ARAB, and the α Chain Variant HB G-Philadelphia. Hemoglobin 17:1, pages 55-66.
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G. P. Tamagnini, P. Gonçalves, M. L. S. Ribeiro, J. Kaeda, F. Kutlar, E. Baysal & T. H. J. Huisman. (1993) β-Thalassehia Mutations in the Portuguese; High Frequencies of Two Alleles in Restricted Populations. Hemoglobin 17:1, pages 31-40.
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W-B. Qin, T-L. Ju, X-L. Yue, X-L. Yan, L-Y. Qin, T. P. Molchanova, D. D. Pobedimskaya & T. H. J. Huisman. (1993) HB A2-Liangcheng [δ117(G19)ASN→ASP(BC→GAC)]: A New δ Chain Variant Detected by Gene Analysis in a Chinese Family. Hemoglobin 17:5, pages 463-466.
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Yu. V. Postnikov, T. P. Molchanova & T. H. J. Huisman. (1993) Allele-Specific Amplification for the Identification of Several Hemoglobin Variants. Hemoglobin 17:5, pages 439-452.
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Y. Yamagishi, K. Ikeda, J. Takahara, S. Irino, H. Hasui, T. Fujiwara, Y. Kaji, T. Harano & K. Harano. (1993) HB J-Guantanamo [α2β2128(H6)ALAASPI Found in a Japanese Family. Hemoglobin 17:4, pages 379-385.
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T. H. J. Huisman, L-H. Gu, J-C. Liu, Y-J. Fei & E. L.D. Walker. (1993) Black α-Thalassemia-1: Partial Characterization of an ∼80 KB Deletion Which Includes the ξ- and α-Globin Genes. Hemoglobin 17:4, pages 345-353.
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K. Adachi, S. Surrey, H. Tamary, J. Kim, H. S. Eck, E. Rappaport & K. Ohene-Frempong. (1993) HB Shelby [β131(H9)GLN→LYS] in Association with HB S [β6(A3)GLU→VAL]: Characterization, Stability, and Effects on HB S Polymerization. Hemoglobin 17:4, pages 329-343.
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V. Divoky, M. Svobodova, K. Indrak, L. Chrobak, T. P. Molchanova & T. H. J. Huisman. (1993) HB Hradec Kralove (HB HK) or α2 β2 115(617)ALA→ASP, A Severely Unstable Hewglobin Variant Resulting in a Dominant β-Thalassemia Trait in a Czech Family. Hemoglobin 17:4, pages 319-328.
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S-S. Chen, K-K. Yang, P-C. Jia, C-C. Liang, M-J. Zhang, M-X. Huang, G-L. Zhang, P-C. Wen & S-K. Du. (1992) A Case of -(4.2)αT/-(4.2)αQ in Combination with a β°-Thalassemia Homozygosity Found in a Family of the Zhuang Nationality in China. Hemoglobin 16:5, pages 409-415.
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T. P. Molchanova, J. B. Wilson, L-H. Gu, R. D. W. Hain, L. S. Chang, A. O. Poon & T. H. J. Huisman. (1992) A Second Observation of the Fetal Methehoglobin Variant HB F-M-Fort Ripley or α2Gγ292(F8)HIS→TYR. Hemoglobin 16:5, pages 389-398.
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W. K. Seltzer, T. C. Abshire, P. A. Lane, J. S. Roloff & J. H. Githed. (1992) Molecular Genetic Studies in Black Families with Sickle Cell Anemia and Unusually High Levels of Fetal Hemoglobin. Hemoglobin 16:5, pages 363-377.
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Y. Hattori, Ku. Yamamoto, Y. Yamashiro, Y. Ohba, S. Miyamura, Ki. Yamamoto, Y. Matsuno, M. Morishita, T. Miyaji & T. Era. (1992) Three β-Thalassemia Mutations in the Japanese: IVS-II-1 (G→A). IVS-II-848 (C→G), and Cooon 90 (GAG→TAG). Hemoglobin 16:1-2, pages 93-97.
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T. Harano, K. Harano, Y. Kushida, K. Imai, R. Nishinakamura & T. Matsunaga. (1992) HB Kodaira [B146(HC3)HIS→GLN]: A New β Chain Variant with an Amino Acid Substitution at the C-Terminus. Hemoglobin 16:1-2, pages 85-91.
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E. George, H-J. Li, Y-J. Fei, A. L. Reese, E. Baysal, B. Cepreganova, J. B. Wilson, L-H. Gu, J. F. Nechtman, T. A. Stoming, J-C. Liu, J. F. Codrington & T. H. J. Huisman. (1992) Types of Thalassemia Among Patients Attending a Large University Clinic in Kuala Lumpur, Malaysia. Hemoglobin 16:1-2, pages 51-66.
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T. A. Cunningham, F. Baker, N. L. Kobrinskyl, B. Cepreganova, E. Baysal, J. B. Wilson & T. H. J. Huiwnan. (1992) The Unstable HB Hammersmith or α2β242(CD1)PHE→SER Observed in an Indian Child; Identification by HPLC AND by Sequence Analysis of Amplified DNA. Hemoglobin 16:1-2, pages 19-25.
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H. Miyashita, K. Hashimoto, H. Mohri, T. Ohokubo, T. Harano, K. Harano & K. Imai. (1992) HB Kanagawa [α40(C5)LYS→MET]: A New α Chain Variant with an Increased Oxygen Affinity. Hemoglobin 16:1-2, pages 1-10.
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Jing-Bo Zhao, Lin Zhao, Y-C. Gu & T. H. J. Huisman. (1992) Types of α-Globin Gene Deficiencies in Chinese Newborn Babies in the Guangxi Region, P.R. China. Hemoglobin 16:4, pages 325-328.
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M. S. Koo, S. I. Kim, H. I. Cho, Y. Hattori, Y. Yamashiro, M. Hoshitani, Y. Ohba, T. Miyaji, Ku. Yamamoto & Ki. Yamamoto. (1992) A β-Thalassemia Mutation Found in Korea. Hemoglobin 16:4, pages 313-320.
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Y. Hattori, Y. Yamashiro, Y. Ohba, T. Miyaji, S. Terai, M. Morishita, Ku. Yamamoto, Ki. Yamamoto, N. Matsumoto & F. Kawano. (1992) Japanese β-Thalassemia [Codon 90 (GAG→TAG)] Has at Least two Origins. Hemoglobin 16:4, pages 303-308.
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Ku. Yamamoto, Ki. Yamamoto, Y. Hattori, Y. Yamashiro, M. Hoshitani, M. Morishita, Y. Ohba, H. Katahira, M. Karasawa, M. Omine, T. Narukiyo, K. Hirabayashi & S. Miyawaki. (1992) Two β-Thalassemia Mutations in Japan: Codon 121 (Gaa→Taa) and IVS-I-130 (G→C). Hemoglobin 16:4, pages 295-302.
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L. Jankovic, A. J. Dimovski, G. D. Efremov & D. Juricic. (1992) A Mutation at CDS 82/83 (-G) Observed in a Yugoslavian Family with a Heterozygosity for β-Thalassemia. Hemoglobin 16:4, pages 291-294.
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M. Ramachandran, L-H. Gu, J. B. Wilson, M. N. Kitundu, A. D. Adekile, J-C. Liu, K. M. McKie & T. H. J. Huisman. (1992) A new Variant, Hb Muscat [α2β232(B14)Leu→val] Observed in Association With Hb S in an Arabian Family. Hemoglobin 16:4, pages 259-266.
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S. Negri Arjona, J. Maldonado Eloy-Garcia, T. P. Molchanova, J. B. Wilson, L. H. Gu & T. H. J. Huisman. (1992) Short Communication Hb Brockton [α2β2138(H16)Ala→Pro] Observed in a Spanish Girl. Hemoglobin 16:6, pages 511-514.
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J. S. Liu, T. P. Molchanova, L. H. Gul, J. B. Wilson, P. Hopmeier, W. Schnedl, E. Balaun, G. J. Krejs & T. H. J. Huisman. (1992) Hb Graz or α2β22(Na2)His→Leu; a new β Chain Variant Observed in four Families from Southern Austria. Hemoglobin 16:6, pages 493-501.
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F. Y. Zeng, S. Fucharoen, S Z Huang & G. P. Rodgers. (1992) Hb Q-Thailand [α74(EF3)Asp→His]: Gene Organization, Molecular Structure, and DNA Diagnosis. Hemoglobin 16:6, pages 481-491.
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G. Schilirò, P. Samperi, C. Consalvo, S. Gangarossa, R. Testa, V. Miraglia & L. Lo Nigro. (1992) Clinical, Hematological, and Molecular Features in Sicilians with Sickle Cell Disease. Hemoglobin 16:6, pages 469-480.
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T. Harano, K. Harano, Y. Kushida & S. Ueda. (1991) A New Abnormal Variant, HB Yahata or β112(G14)CYS→TYR, Found in a Japanese: Structural Confirmation by DNA Sequencing of the β-Globin Gene. Hemoglobin 15:1-2, pages 109-113.
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H-W. Li, J. F. Codrington, G. Schiliro, L. D. Wadsworth, Ph. Beris, A. Adekile & T. H.J. Huisman. (1991) The Usefulness of Sequence Analysis of Amplified DNA for the Identification of δ Chain Variants. Hemoglobin 15:1-2, pages 77-84.
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R. Öner, S. Agarwal, A. J. Dimovski, G. D. Efremov, G. H. Petkov, C. Altay, A. Gurgey & T. H.J. Huisman. (1991) The G→A Mutation at Position +22 31 to the Cap Site of the β-Globin Gene as a Possible Cause for a β-Thalassemia. Hemoglobin 15:1-2, pages 67-76.
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P. Fortina, K. Delgrosso, E. Werner, K. Haines, E. Rappaport, E. Schwartz & S. Surrey. (1991) A > 200 kb deletion removing the entire β-like globin gene cluster in a family of Irish Descent. Hemoglobin 15:1-2, pages 23-41.
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S. Fattoum, F. Guemira, C. Öner, R. Öner, H-W. Li, F. Kutlar & T. H.J. Huisman. (1991) β-Thalassemia, HB S-β-Thalassemia and Sickle Cell Anemia Among Tunisians. Hemoglobin 15:1-2, pages 11-21.
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S. Abbes, S. Fattoun, N. Vidaud, M. Goossens & J. Rosa. (1991) Sickle Cell Anemia in the Tunisian Population: Haplotyping and HB F Expression. Hemoglobin 15:1-2, pages 1-9.
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D. Plašeska, A. J. Dimovski, L. Janković, E. Šukarova, G. D. Efremov, E. Gebauer & D. Jeranće. (1991) HB Hoshida [β43(CD2)GLU→GLN] Observed in a Yugoslavian Family. Hemoglobin 15:6, pages 541-543.
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G. P. Tamagnini, M. L. Ribeiro, V. Valente, M. Ramachandran, J. B. Wilson, E. Baysal, L-H. Gu & T. H. J. Huisman. (1991) HB Coimbra or α2β299(Gl)ASP→GLU, A Newly Discovered High Oxygen Affinity Variant. Hemoglobin 15:6, pages 487-496.
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M. M. Keeling, S. J. Bertolone, E. Baysal, Y-C. Gu, B. Cepreganova, J. B. Wilson & T. H. J. Huisman. (1991) HB Mizuho or α2β268(E12)Leu→pro in a Caucasian Boy with high levels of HB F; Identification by Sequencing of Amplified DNA. Hemoglobin 15:6, pages 477-485.
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D. Plašeska, L. Janković, A. J. Dimovski, D. Milenović, D. Jurišić & G. D. Efremov. (1991) HB Yokohama [β31(B13)LEU→PRO] Detected AS A de novo Mutation in a Yugoslavian Boy. Hemoglobin 15:6, pages 469-476.
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M. Boussiou, D. Loukopoulos, J. Christakis & Ph. Fessas. (1991) The Origin of the Sickle Mutation in Greece; Evidence from βS Globin Gene Cluster Polymorphisms. Hemoglobin 15:6, pages 459-467.
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Y. Hattori, Y. Yamashiro, Y. Ohba, T. Miyaji, M. Morishita, Ku. Yamamoto, Ki. Yamamoto, S. Narai & A. Kimura. (1991) A New β-Thalassemia Mutation (Initiation Codon ATG→GTG) Found in the Japanese Population. Hemoglobin 15:4, pages 317-325.
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Y-C. Gu, L-H. Gu, J. B. Wilson, B. Cepreganova, M. Ramachandran, E. L.D. Walker, T. H. J. Huisman & P. Potitong. (1991) Hb Westmead [α122(H5)HIS→GLN], Hb E [β26(B8)6Ll→LYS], and α-Thamssemia-2 (3.7 KB Deletion) in a Laotian Family. Hemoglobin 15:4, pages 297-302.
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T. Harano, K. Harano, Y. Kushida, S. Ueda, A. Yoshii & M. Nishinarita. (1991) Hb Isehara (or Hb Redondo) [β92(F8)HIS→SN]: An Unstable Variant with a Proximal Histidine Substitution at the Heme Contact. Hemoglobin 15:4, pages 279-290.
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R. B. Gupta, R. S. Tiwary, P. L. Pande, F. Kutlar, C. Öner, R. Öner & T. H. J. Huisman. (1991) Hemoglobinopathies Among the Gond Tribal Groups of Central India; Interaction of α- and β-Thalassemia with β Chain Variants. Hemoglobin 15:5, pages 441-458.
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S. K. Ballas, C. A. Talacki, K. Adachi, E. Schwartz, S. Surrey & E. Rappaport. (1991) The XMN I Site (-158, C→T) 5′ to ttle Gγ GENE: Correlation with the Senegalese Haplotype and Gγ Globin Expression. Hemoglobin 15:5, pages 393-405.
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F. Fernandez-Rachubinski, W. W. Murray, M. A. Blajchman & R. A. Rachubinski. (1990) Incorporation of 7-deaza dGTP during the amplification step in the polymerase chain reaction procedure improves subsequent DNA sequencing. DNA Sequence 1:2, pages 137-140.
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. (1990) Low Quantities of Hb Boyle Heights or α26(A4)ASP→Oβ2 Observed in Three Members of a Caucasian Family. Hemoglobin 14:6, pages 637-640.
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W. Zhao, J. B. Wilson, B. B. Webber, A. Kutlar, G. P. Tamagnini, B. Kuan & T. H. J. Huisnan. (1990) Hb Hekinan Observed in Three Chinese from Macau; Identification of the Gag→Gat Mutation in the αl-Globin Gene. Hemoglobin 14:6, pages 627-635.
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D. Plaseska, F. Kutlar, J. B. Wilson, Y. J. Fei & T. H. J. Huisman. (1990) Hb F-Charlotte, an Aγ Variant with a Threonine Residue in Position γ75 and a Glycine Residue in Position γ136. Hemoglobin 14:6, pages 617-625.
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T. Harano, K. Harano, S. Ueda, K. Imai & S. Marubashi. (1990) Hb Yamagata [B132(H10)LYS-ASN]: A New Abnormal Hemoglobin in a Japanese Family. Hemoglobin 14:2, pages 207-211.
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L. Jankovic, G. D. Efremov, O. Josifovska, D. Juricic, T. A. Stomingl, A. Kutlar & T. H. J. Huisman. (1990) An Initiation Codon Mutation as a Cause of a β-Thalassemia. Hemoglobin 14:2, pages 169-176.
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Y. Hattori, M. Morishita, Y. Yamashiro, Ki. Yamamoto, Ku. Yamamoto, Y. Matsuno, Y. Ohba & T. Miyaji. (1990) Three Japanese Families with Hb H Disease: Gene Anals and Their Characterizations. Hemoglobin 14:5, pages 559-567.
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M. Harkness, D. R. Harkness, F. Kutlar, A. Kutlar, J. B. Wilson, B. B. Webber, J. F. Codrington & T. H.J. Huisman. (1990) Hb Sun Prae or α213o(H13)Ala → Proβ2 A New Unstable Variant Occurring In Low Quantities. Hemoglobin 14:5, pages 479-489.
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C. A. Talacki, E. Rappaport, E. Schwartz, S. Surrey & S. K. Ballas. (1990) β-Globin Gene Cluster Haplotypes Inhbc Heterozygotes. Hemoglobin 14:3, pages 229-240.
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R. Öner, C. Altay, A. Gurgey, M. Aksoy, Y. Kilinc, T. A. Stoming, A. L. Reese, A. Kutlar, F. Kutlar & T. H. J. Huisman. (1990) β-Thalassemia in Turkey. Hemoglobin 14:1, pages 1-13.
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W. A. Schroeder, Darleen R. Powars, Lois M. Kay, Linda S. Chan, Van Huynh, Joan B. Shelton & J. Roger Shelton. (1989) β-Cluster Haplotypes, α-Gene Status, and Hematological Data from SS, SC, and S-β-Thalassemia Patients in Southern California. Hemoglobin 13:4, pages 325-353.
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Y. Yamashiro, Y. Hattori, Y. Matsuno, Y. Ohba, T. Miyaji, Ki. Yamamoto, Ku. Yamamoto, Y. Nakayama & Y. Abe. (1989) Another Example of Japaneseβ-Thalassemia [-31 CAP (A→ G)]. Hemoglobin 13:7-8, pages 761-767.
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Y. Hattori, A. Yamane, Y. Yamashiro, Y. Matsuno, Ki. Yammoto, Ku. Yamamoto, Y. Ohba & T. Miyaji. (1989) Characterization of β-Thalassemia Mutations Among the Japanese. Hemoglobin 13:7-8, pages 657-670.
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Samir K. Ballas, Carol A. Talacki, Vijay M. Rao & Robert M. Steiner. (1989) The Prevalence of Avascular Necrosis in Sickle Cell Anemia: Correlation with α-Thalassemia. Hemoglobin 13:7-8, pages 649-655.
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T. Harano, K. Harano, K. Imai, T. Ohnishi & T. Akabori. (1989) HB J-Calabria [β64(E8)GLY→ASP] Found in a Japanese Family. Hemoglobin 13:2, pages 185-188.
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T. Harano, K. Harano, K. Imai, H. Yunoki, H. Yagi, K. Nagashima & T. Kuroume. (1989) HB J-Meerut [α120(H3)ALA→GLU] Found in a Japanese Family. Hemoglobin 13:2, pages 169-175.
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J. M. Gonzalez-Redondo, F. Gilsanz & P. Ricard. (1989) Characterization of a New α-Thalassemia-1 Deletion in a Spanish Family. Hemoglobin 13:2, pages 103-116.
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J. M. Gonzalez-Redondo, T. A. Stoming, F. Kutlar, A. Kutlar, H. Hu, J. B. Wilson & T. H. J. Huisman. (1989) HB Monroe or α2β230(B12)ARG→THR, a Variant Associated with β-Thalassemia due to a G→C Substitution Adjacent to the Donor Splice Site of the First Intron. Hemoglobin 13:1, pages 67-74.
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Y. J. Fei, F. Kutlar, H. F. Harris, M. M. Wilson, A. Milana, P. Sciacca, G. Schiliro, B. Masaia, L. Manca, Ç Altay, A. Gurgey, J. Ma. de Pablos, A. Villegas & T. H. J. Huisman. (1989) A Search for Anomalies in the ζ,α,β, and γ Globin Gene Arrangements in Normal Black, Italian, Turkish, and Spanish Newborns. Hemoglobin 13:1, pages 45-65.
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A. Kutlar, F. Kutlar, M. Aksoy, A. Gurgey, Ç. Altay, J. B. Wilson, J. C. Diaz-Chico, H. Hu & T. H. J. Huisman. (1989) β-Thalassemia Intermedia in Two Turkish Families is Caused by the Interaction of HB Knossos [β27(B9)ALA→SER] and of HB City of hope [β69(E13)Gly→Ser] with B°-Thalassemia. Hemoglobin 13:1, pages 7-16.
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S. C. Wong, T. A. Stoming, G. D. Efremov & T. H. J. Huisman. (1989) High Frequencies of a Rearrangement (+ATA; -T) at -530 to the β-Globin Gene in Different Populations Indicate the Absence of a Correlation with a Silent β-Thalassemia Determinant. Hemoglobin 13:1, pages 1-5.
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P. Kollia, J. M. Gonzalez-Redondo, T. A. Stoming, D. Loukopoulos, C. Politis & T. H. J. Huisman. (1989) Frameshift Codon 5 [FSC-5 (−CT)] Thalassemia; a Novel Mutation Detected in a Greek Patient. Hemoglobin 13:6, pages 597-604.
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J. B. Wilson, B. B. Webber, A. Kutlar, A. L. Reese, V. C. McKie, C. L. Lutcher, A. E. Felice & T. H. J. Huisman. (1989) Hb Evans or α262(E11)Val→Metβ2; an Unstable Hemoglobin Causing a Mild Hemolytic Anemia. Hemoglobin 13:6, pages 557-566.
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J. F. Codrington, F. A. Codrington, J. H. Wisse, J. B. Wilson, B. B. Webber, S. C. Wong & T. H. J. Huisman. (1989) Hb Chad or α223(B4)GLU→LYSβ2 Observed in Members of a Surinam Family in Association with α-Thalassemia-2 and with HB S. Hemoglobin 13:6, pages 543-556.
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Bruce Sharon, Mortirner Poncz, Saul Surrey & Elias Schwartz. (1988) Non-Random Association of the ma I Polymorphic Site 5′ to the β-Globin Gene with Major Sickle Cell Haplotypes. Hemoglobin 12:2, pages 115-124.
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S. Liang, Z. Tang, C. Su, Q. Lung, R. Liang, Y. J. Fei, F. Kutlar, J. B. Wilson, B. B. Mebber, H. Hu & T. H. J. Huisman. (1988) HB Duan [α75(EF4)ASP→ALA), HB Westmead [α122(H5)HIS→GLN], and α-Thalassemia-2 (-4.2 KB Deletion) in a Chinese Family. Hemoglobin 12:1, pages 13-21.
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L. Manca, B. Masala, M. Orzalesi, H. J. Huang & T. H. J. Huisman. (1988) Abnormal γ-Globin Gene Arrangements in Sardinians. Hemoglobin 12:5-6, pages 741-753.
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T. Harano, K. Harano, H. Ukita, Y. Wada, A. Hayashi, Y. Ohba, T. Miyaji, F. Kutlar & T. H. J. Huisman. (1988) Characterization of Abnormalities in the γ-Globin Gene Arrangements of Japanese Newborns. Hemoglobin 12:5-6, pages 723-739.
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B. Masala, L. Manca, D. Gallisai, A. Stangoni, K. D. Lanclos, F. Kutlar, K. G. Yang & T. H. J. Huisnan. (1988) Biochemical and Molecular Aspects of β-Thalassemia Types in Northern Sardinia. Hemoglobin 12:5-6, pages 661-671.
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Abraham Fainsod, Gill Diamond, Menashe Marcus & Frank H. Ruddle. (1987) Cloning of a Human S-Phase Cell Cycle Gene: Use of Transient Expression for Screening. Molecular and Cellular Biology 7:2, pages 775-779.
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Y. Ohba, K. Yamaoto, Y. Hattori, R. Kawata & T. Miyaji. (1987) Hyperunstable Hemoglobin Toyama [α2136(H19)LEU→ARGβ2]: Detection and Identification by in Vitro Biosynthesis with Radioactive Amino Acids. Hemoglobin 11:6, pages 539-556.
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T. Harano, K. Harano, S. Ueda & K. Nakaya. (1987) HB D Los Angeles [β121 Glu →] in Japan. Hemoglobin 11:2, pages 177-180.
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Z. F. Chu, C. C. Liang, F. Kutalar & T. H.J. Huisman. (1987) Fetal Hemoglobin Heterogeneity in Chinese Newborns of the Uygur and Han Nationalities; Comparisons of Babies from Xinjiang and Beijing. Hemoglobin 11:2, pages 123-128.
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K. Shimizu. (1987) DNA Polymorphism Patterns in the β-Globin Gene Cluster in the Japanese Population. Hemoglobin 11:5, pages 487-496.
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Y. Hattori, F. Kutlar, C. J. Mosley, S. M. Mayson & T. H. J. Huisman. (1986) Association of the level of Gγ chain in the fetal hemoglobin of normal adults with specific haplotypes. Hemoglobin 10:2, pages 185-204.
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Y. Hattori, F. Kutlar, A. Kutlar, V. C. McKie & T. H. J. Huisman. (1986) Haplotypes of βS Chromosomes Among Patients with Sickle Cell Anemia from Georgia. Hemoglobin 10:6, pages 623-642.
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J. E. Bowman, R. Bloom, S. S. Chen, B. B. Webber, J. B. Wilson, F. Kutlar, A. Kutlar & T. B. J. Huisman. (1986) Hb Chicago or α2136(H19)LEU+METβ2 and A-Gγ-GGMGlobin GWE Arrangewznt in a Black Family. Hemoglobin 10:5, pages 495-505.
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K. D. Lanclos, A. Kutlar, F. Kutlar, P. J. Ojwang, A. L. Reese & T. H. J. Huisman. (1986) The Effect of α-Thalassemia on the Level of Hybrid Hemoglobin Variants in Heterozygotes. Hemoglobin 10:4, pages 401-416.
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K. Faridah, E. George, R. J. Trent, B. J. Padanilam, H-J. J. Huang & T. H. J. Huisman. (1986) Homozygosity for a New Type of Gγ(Aγδβ)°-Thalassemia in a Malaysian Male. Hemoglobin 10:4, pages 353-363.
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