Hb I Trait in an Algerian Mussulman Family, Presenting Two Abnormal Components-Reference-Cited by-同舟云学术

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Hb I Trait in an Algerian Mussulman Family, Presenting Two Abnormal Components

Published:1961-12-01 Issue:6 Volume:18 Page:750-757
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Boulard Cl.¹,Cosset A.²,Destaing F.²,Duzer A.²,Jonxis J. H. P.³,Muller C. J.⁴,Portier A.⁵

Affiliation:

1. Pathologie Genérale et Médicale de la Faculté de Médicine d'Algèr, Algeria.

2. Département du Pathologie Genérale et Médicale de la Faculté de Médicine d'Algèr, Algeria.

3. State University, Groningen, The Netherlands.

4. Department of Pediatrics, State University, Groningen. The Netherlands.

5. Le Laboratoire Central d'Hématologie-Bactériologie du Centre Hospitalier Regional d'Algèr, Algeria.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/18/6/750/751766/750.pdf

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hb I α16 Lys →Glu and Hb Broussais α90 Lys →Asn in Australian families;Pathology;1978

2. Hemoglobin I in a white family in Saskatoon;Clinical Biochemistry;1971-04

3. Diminished synthesis of an alpha chain mutant, hemoglobin I (α16 lys → glu);Journal of Clinical Investigation;1970-12-01

4. Reifungsstörungen der Erythropoese: Quantitative und qualitative Störungen der Hämoglobinproduktion;Erkrankungen der Stützgewebe Erkrankungen des Blutes und der Blutbildenden Organe;1967

5. The Characterization of Hemoglobin Shimonoseki;Blood;1964-11-01

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