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Hemoglobin
international journal for hemoglobin research
Volume 9, 1985 - Issue 5
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Original Article

Hb Lepore-Hb C and Hb Lepore-β°-Thalassemia Compound Heterozygotes1 N an Algerian Family

A. Francina Groupe de Recherches sur le Globule Rouge, Faculté de Medicine Grange-Blanche, 69373, Lyon Cedex 08, France
,
S. Elwan Groupe de Recherches sur le Globule Rouge, Faculté de Medicine Grange-Blanche, 69373, Lyon Cedex 08, France
,
F. Baklouti Groupe de Recherches sur le Globule Rouge, Faculté de Medicine Grange-Blanche, 69373, Lyon Cedex 08, France
,
J. Delaunay Groupe de Recherches sur le Globule Rouge, Faculté de Medicine Grange-Blanche, 69373, Lyon Cedex 08, France
,
E. Dorleac Hopital Edouard Herriot, 69374, Lyon Cedex 08, France
,
M. Aubry Hopital Edouard Herriot, 69374, Lyon Cedex 08, France
,
L. Roda Centre Hospitalier d'Annecy, 74000, Annecy, France
&
N. Phillipe Hôpital Debrousse, 69322, Lyon Cedex 1, France
 show all
Pages 505-508 | Received 12 Apr 1985, Accepted 29 Jul 1985, Published online: 07 Jul 2009

Citations (3)

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Read on this site (1)

G. Bozkurt, E. Baysal, L-H. Gu & T. H.J. Huisman. (1994) Thalassemia intermedia in two patients with Hb lepore-β°-thalassemia (Frameshift codon 8, -AA). Hemoglobin 18:3, pages 247-250.
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Articles from other publishers (2)

D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Faouzi Baklouti, Alain Francina, Evelyne Dorléac, Véronique Baudin‐Chich, Germaine Gombaud‐Saintonge, Henri Plauchu, Henri Wajcman, Jean Delaunay & Jacqueline Godet. (2006) Asymptomatic association of hemoglobin Dunn (α6[A4]Asp→Asn) and hemoglobin O‐Arab (β121[GH4]Glu→Lys) in a Moroccan man. American Journal of Hematology 27:4, pages 253-256.
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