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Hemoglobin
international journal for hemoglobin research
Volume 23, 1999 - Issue 1
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Original Article

The association of Hb khartoum [β124(H2)Pro→Arg] with γ+-thalassemia is responsible for hemolytic disease in the newborn of a sudanese family

R. A. Bayoumi College of Medicine, Sultan Qaboos University, Muscat, OmanCorrespondence[email protected]
,
A. Dawodu Faculty of Medicine and Health Sciences United Arab Emirates University, Al-Ain, United Arab Emirates
,
M. M. Qureshi Faculty of Medicine and Health Sciences United Arab Emirates University, Al-Ain, United Arab Emirates
,
A. Al-Khider Al-Ain and Tawam Hospitals, Ministry of Health, Al-Ain, United Arab Emirates
,
P. Fitzgerald Al-Ain and Tawam Hospitals, Ministry of Health, Al-Ain, United Arab EmiratesView further author information
,
J. Riou Department of Biochemistry, Hôpital Henri Mondor, Créteil, France
,
C. A. Fisher Institute of Molecular Medicine, John Radcliffe Hospital Headington, Oxford, United Kingdom
,
A. Fitches Institute of Molecular Medicine, John Radcliffe Hospital Headington, Oxford, United Kingdom
&
J. M. Old Institute of Molecular Medicine, John Radcliffe Hospital Headington, Oxford, United Kingdom
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Pages 33-45 | Received 30 May 1997, Accepted 28 Aug 1998, Published online: 05 Aug 2009

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