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Hemoglobin
international journal for hemoglobin research
Volume 30, 2006 - Issue 2
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SHORT COMMUNICATION

A New α Chain Hemoglobin Variant: Hb Al-Hammadi Riyadh [α75(EF4)Asp→Val (α2)]

Nelly Burnichon Unité de Pathologie Moléculaire, Fédération de Biochimie et de Biologie Spécialisée, Hôpital Edouard Herriot, Lyon, France
,
Philippe Lacan Unité de Pathologie Moléculaire, Fédération de Biochimie et de Biologie Spécialisée, Hôpital Edouard Herriot, Lyon, France
,
Michel Becchi Institut de Biologie et Chimie des Protéines (IFR128), Lyon, France
,
Isabelle Zanella-Cleon Institut de Biologie et Chimie des Protéines (IFR128), Lyon, France
,
Martine Aubry Unité de Pathologie Moléculaire, Fédération de Biochimie et de Biologie Spécialisée, Hôpital Edouard Herriot, Lyon, France
,
Mohammed Mowafy Laboratory Department, Al-Hammadi Hospital, Riyadh, Kingdom of Saudi Arabia
,
Nicole Couprie Laboratoire Marcel Mérieux, Lyon, France
&
Alain Francina Unité de Pathologie Moléculaire, Fédération de Biochimie et de Biologie Spécialisée, Hôpital Edouard Herriot, Lyon, FranceCorrespondence[email protected]
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Pages 155-164 | Received 04 Oct 2005, Accepted 02 Nov 2005, Published online: 07 Jul 2009

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Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
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Articles from other publishers (3)

Liu Du, Hong-Ning Xie, Lin-Huan Huang, Ying-Jun Xie & Li-Hong Wu. (2016) Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with ventricular septal defects by chromosomal microarray-based analysis. Prenatal Diagnosis 36:13, pages 1178-1184.
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Zuhair N. Al-Hassnan & Nadia Sakati. 2010. Genetic Disorders Among Arab Populations. Genetic Disorders Among Arab Populations 531 573 .
Isabelle Zanella-Cleon, Philippe Joly, Michel Becchi & Alain Francina. (2009) Phenotype determination of hemoglobinopathies by mass spectrometry. Clinical Biochemistry 42:18, pages 1807-1817.
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