The levels of ?, ?, and ? chains in patients with Hb H disease-Reference-Cited by-同舟云学术

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The levels of ?, ?, and ? chains in patients with Hb H disease

Published:1989-05 Issue:2 Volume:82 Page:179-186
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Kutlar Ferdane,Gonzalez-Redondo Jose M.,Kutlar Abdullah,Gurgey Aytemiz,Altay �igdem,Efremov Georgi D.,Kleman Klara,Huisman Titus H. J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00284054.pdf

Reference38 articles.

1. Adams JG III, Coleman MB, Hayes J, Morrison WT, Steinberg MH (1985) Modulation of fetal hemoglobin synthesis by iron deficiency. N Engl J Med 28:1402?1405

2. Altay C, Gurgey A, Tuncbilek E (1980) Hematological evaluation of patients with various combinations of ?-thalassemia. Am J Hematol 9:261?267

3. Bakioglu I, Hattori Y, Kutlar A, Mathew C, Huisman THJ (1985) Five adults with mild sickle cell anemia share a ?S chromosome with the same haplotype. Am J Hematol 20:297?300

4. Betke K, Marti HR, Schlicht I (1959) Estimation of small percentages of foetal haemoglobin. Nature 184:1877?1878

5. Bunn HF, Forget BG (1986) Hemoglobin: molecular, genetic and clinical aspects. Saunders, Philadelphia

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