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Hemoglobin
international journal for hemoglobin research
Volume 9, 1985 - Issue 1
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Original Article

Homozygous Hbe and Hbse Disease in a Saudi Family

M. J. Hardy Department of Laboratory Medicine, King Fahd Armed Forces Hospital, PO Box 9862, Jeddah, 21159, Saudi Arabia
&
M. S. Ragbeer Department of Laboratory Medicine, King Fahd Armed Forces Hospital, PO Box 9862, Jeddah, 21159, Saudi Arabia
Pages 47-52 | Received 07 Sep 1984, Accepted 07 Dec 1984, Published online: 07 Jul 2009

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Snehadhini Dehury, Pradeep K. Mohanty, Siris Patel, Satyabrata Meher, Kishalaya Das, Prasanta Purohit, Sarmila Sahoo & Jagnyeswar Ratha. (2021) Profiling of 35 Cases of Hb S/Hb E (HBB: c.20A>T/HBB: c.79G>a), Disease and Association with α-Thalassemia and β-Globin Gene Cluster Haplotypes from Odisha, India. Hemoglobin 45:6, pages 380-386.
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D. M. Pillers, M. Jones, C. Head & R. T. Jones. (1992) HB Hope [B136(H14)GLY→ASP] and HB E [D26 (B8) GLU→LYS] : Compound Heterozygosity in a Thai Mien Family. Hemoglobin 16:1-2, pages 81-84.
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Articles from other publishers (9)

Ibrahim Khamees, Fateen Ata, Hassan Choudry, Ashraf T. Soliman, Vincenzo De Sanctis & Mohamed A. Yassin. (2021) Manifestations of HbSE sickle cell disease: a systematic review. Journal of Translational Medicine 19:1.
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Usman Tauseef, Misbah Anjum, Mohsina Ibrahim, Hina Sabih Baqai, Abubakar Tauseef, Marium Tauseef, Muhammad Sohaib Asghar, Maryam Zafar, Uzma Rasheed & Nimra Shaikh. (2021) OCCURRENCE OF UNUSUAL HAEMOGLOBINOPATHIES IN BALOCHISTAN: HB SD AND HB SE - PRESENTATION WITH OSTEOMYELITIS. Revista Paulista de Pediatria 39.
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Elise K. Burton. (2019) Red Crescents: Race, Genetics, and Sickle Cell Disease in the Middle East. Isis 110:2, pages 250-269.
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María Belén Paredes & María Eugenia Sulen. (2019) Sickle Cell Anemia: A review on the most severe form of Sickle Cell Disease. Bionatura 02:Bionatura Conference Serie.
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H. H. M. KNOX-MACAULAY, M. M. AHMED, D. GRAVELL, S. AL-KINDI & A. GANESH. (2007) Sickle cell?haemoglobin E (HbSE) compound heterozygosity: a clinical and haematological study. International Journal of Laboratory Hematology 29:4, pages 292-301.
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David Masiello, Matthew M. Heeney, Adeboye H. Adewoye, Shawn H. Eung, Hong‐Yuan Luo, Martin H. Steinberg & David. H.K. Chui. (2007) Hemoglobin SE disease—A concise review. American Journal of Hematology 82:7, pages 643-649.
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Pravas Mishra, H. P. Pati, Tathagat Chatterjee, Ashish Dixit, Dharma R. Choudhary, M. Upendra Srinivas, Manoranjan Mahapatra & V. P. Choudhry. (2005) Hb SE disease: a clinico-hematological profile. Annals of Hematology 84:10, pages 667-670.
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Kathy S. Rey, Carol A. Unger, Sreedhar P. Rao & Scott T. Miller. (1991) Sickle cell-hemoglobin E disease: Clinical findings and implications. The Journal of Pediatrics 119:6, pages 949-951.
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J. R. Aluoch, Y. Kilinç, M. Aksoy, G. T. Yüregir, I. Bakioglu, A. Kutlar, F. Kutlar & T. H. J. Huisman. (1986) Sickle cell anaemia among Eti-Turks: haematological, clinical and genetic observations. British Journal of Haematology 64:1, pages 45-55.
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