Citations (23)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (7)
T. Harano, K. Harano & T. Katsuki. (1995) Hb yaizu [β79(EF3)Asp → Asn]: A new β chain variant found in a japanese female. Hemoglobin 19:1-2, pages 21-25.
Read now
Read now
E. G. Kazanetz, J. Ye. Leonova, J. B. Wilson, S. K. McMillan, M. Walbrecht, J. Mi. de Pablos Gallego & T. H. J. Huisman. (1995) Hb ananosa or α2111(G18)Ala → Valβ (α2 Mutation) and Hb mulhacen or α2123(H6)Ala → Serβ2 (αl Mutation) are two silent stable variants detected by sequencing of amplified dna. Hemoglobin 19:1-2, pages 1-6.
Read now
Read now
T. Harano, K. Harano, K. Imai, T. Murakami & H. Matsubara. (1995) HB Kurosaki [α7(A5)LYS→GLU]: A New α Chain Variant Found in a Japanese Woman. Hemoglobin 19:3-4, pages 197-201.
Read now
Read now
M. A. Rosenthal, T. A. Campbell & N. Epstein. (1995) Binding Specificity of a Monoclonal Antibody to Human Hb A. Hemoglobin 19:3-4, pages 191-196.
Read now
Read now
S. Abbes, P. A. Fitzgerald, E. Varady, R. Girot, P. Pic, Y. Blouquit, R. Ducrocq, F. Drupt & H. Wajcman. (1995) Two Fetal Hemoglobin Variants Affecting the Same Residue: HB F-Emirates [Gγ59(E3)LYS→GLU] and HB F-Sacromonte [Gγ59(E3)LYS→GLN]. Hemoglobin 19:3-4, pages 173-182.
Read now
Read now
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.
Read now
Read now
K. Krishnan, F. Martinez, R. T. Wille, R. T. Jones, D. T. Shin, C. Head, V. F. Fairbanks & L. Dabich. (1994) HB Washtenaw [βT11(A8)VAL-PHE]: An Electrophoretically Silent, Unstable, Low Oxygen Affinity Variant Associated with Anemia and Chronic Cyanosis. Hemoglobin 18:4-5, pages 285-295.
Read now
Read now
Articles from other publishers (16)
Gülçin ŞAHİNGÖZ ERDAL, Murat KOŞER, Pınar KASAPOĞLU & Nilgün IŞIKSAÇAN. (2019) Hemoglobinopati, Asetil Salisilik Asit Kullanimi Ve Üreminin İmmünoturbidimetrik Ve HPLC Hemoglobin A1c Ölçümleri Üzerine Etkileri. Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi 6:3, pages 142-147.
Crossref
Crossref
Katsumi Iizuka, Masami Mizuno, Hiroyuki Niwa & Jun Takeda. (2015) A Rare Case of Variant Hemoglobin (Hb Yahata) Suspected Based on Inconsistent Plasma Glucose and HbA1c Levels. Internal Medicine 54:14, pages 1771-1775.
Crossref
Crossref
Chih-Hsun Chu, Hing-Chung Lam, Jenn-Kuen Lee, Mei-Chun Wang, Chih-Chen Lu, Chun-Chin Sun & Ming-Ju Chuang. (2009) Common Hemoglobin Variants in Southern Taiwan and Their Effect on the Determination of HbA1c by Ion-exchange High-performance Liquid Chromatography. Journal of the Chinese Medical Association 72:7, pages 362-367.
Crossref
Crossref
T. M. Reynolds, P. J. Twomey, T. C. Harvey & B. N. Green. (2004) The number of unexpected HbA1c variants may be a greater problem in routine practice than is generally realized. Diabetic Medicine 21:9, pages 1041-1044.
Crossref
Crossref
Ponthenkandath Sasidharan. (2004) An approach to diagnosis and management of cyanosis and tachypnea in term infants. Pediatric Clinics of North America 51:4, pages 999-1021.
Crossref
Crossref
Regine Witkowski, Otto Prokop, Eva Ullrich & Gundula ThielRegine Witkowski, Otto Prokop, Eva Ullrich & Gundula Thiel. 2003. Lexikon der Syndrome und Fehlbildungen. Lexikon der Syndrome und Fehlbildungen
31
1336
.
Lynn Bry, Philip C Chen & David B Sacks. (2001) Effects of Hemoglobin Variants and Chemically Modified Derivatives on Assays for Glycohemoglobin. Clinical Chemistry 47:2, pages 153-163.
Crossref
Crossref
Regine Witkowski, Otto Prokop & Eva UllrichRegine Witkowski, Otto Prokop & Eva Ullrich. 1999. Lexikon der Syndrome und Fehlbildungen. Lexikon der Syndrome und Fehlbildungen
35
1198
.
Naoyuki Takahata & Yoko Satta. 1998. Mutation and Evolution. Mutation and Evolution
157
169
.
Poluru L. Reddy & Lemuel J. Bowie. (1997) Sequence-Based Diagnosis of Hemoglobinopathies in the Clinical Laboratory. Clinics in Laboratory Medicine 17:1, pages 85-96.
Crossref
Crossref
Danielle Promé, Catherine Deon, Jean-Claude Promé, Henri Wajcman, Frédéric Galacteros & Yves Blouquit. (1996) Use of combined mass spectrometry methods for the characterization of a new variant of human hemoglobin: The double mutant hemoglobin villeparisis β77(EF1) His → Tyr, β 80 (EF4) Asn → Ser. Journal of the American Society for Mass Spectrometry 7:2, pages 163-167.
Crossref
Crossref
Britta Landin, Stig Berglund & Kristina Wallman. (1996) Two different mutations in codon 97 of the β-globin gene cause Hb Malmö in Sweden. American Journal of Hematology 51:1, pages 32-36.
Crossref
Crossref
W. J. Schnedl, E. C. Reisinger, R. W. Lipp, P. Hopmeier & G. J. Krejs. (1995) Hemoglobin variants recently detected in Austria. Annals of Hematology 71:4, pages 185-187.
Crossref
Crossref
Mudra Kohli‐Kumar, Theodore Zwerdling & Donald L. Rucknagel. (2006)
Hemoglobin F‐Cincinnati, α
2
G
γ
2
41(C7) Phe → Ser in a newborn with cyanosis
. American Journal of Hematology 49:1, pages 43-47.
Crossref
Crossref
N. Akar, A. Özden, E. Akar, S. Cin & A. Arcasoy. (2006) Discrimination of Hb D Los Angeles (B121 Glu‐Gln) and Hb Beograd (B121 Glu‐Val) by Dual Restriction Enzyme Analysis. American Journal of Hematology 48:4, pages 280-281.
Crossref
Crossref
Regine Witkowski, Otto Prokop & Eva UllrichRegine Witkowski, Otto Prokop & Eva Ullrich. 1995. Lexikon der Syndrome und Fehlbildungen. Lexikon der Syndrome und Fehlbildungen
608
696
.