Hb J Baltimore (β 16 (A13) Gly ↣ Asp) in Association with β-Thalassemia in a Sicilian Family-Reference-Cited by-同舟云学术

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Hb J Baltimore (β 16 (A13) Gly ↣ Asp) in Association with β-Thalassemia in a Sicilian Family

Published:1979-01 Issue:6 Volume:3 Page:459-464
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Musumeci S.,Schiliro G.,Fisher A.,Musco A.,Maritiucci M.,Mavilio F.,Fontanarosa P. P.,Tentori L.

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630267909002282

Reference13 articles.

1. Rapid electrophoresis and quantitation of haemoglobins on cellulose acetate

2. Estimation of Small Percentages of Fœtal Hæmoglobin

3. Hemoglobin Legnano (α2141 (HC3) Arg → Leu β2): A New Abnormal Human Hemoglobin with High Oxygen Affinity

Cited by 4 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 J-Baltimore [β16(A13)GLY→ASP] Associated with β+Thalassemia in a Spanish Family;Hemoglobin;1996-01

2. Hemoglobin J-Baltimore (β16(A13)Gly → Asp): Interference with the assay of HbA1c;Clinica Chimica Acta;1987-09

3. First Association in Spain of Hb J Baltimore Alpha A2 Beta216 (A13) GLY→asp and Beta° Thalassemia;Hemoglobin;1982-01

4. Globin Chain Synthesis in Hb J Baltimore-β+-Thalassemia;American Journal of Clinical Pathology;1981-06-01

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