Hb TAYBE: clinical and morphological findings IN 43 patients-Reference-Cited by-同舟云学术

Hb TAYBE: clinical and morphological findings IN 43 patients

Published:2015-12-15 Issue:2 Volume:97 Page:137-144
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:Eur J Haematol

Author:

Koren Ariel¹²,Levin Carina¹²,Zalman Luci³,Palmor Haya³,Filon Dvora⁴,Chubar Evgeny⁵,Resnitzky Peretz⁶,Bennett Michael²³⁵

Affiliation:

1. Pediatric Hematology Unit; Emek Medical Center; Afula Israel

2. The Ruth and Baruch Rappaport School of Medicine; Technion; Israel Institute of Technology; Haifa Israel

3. Hematology Laboratory; Emek Medical Center; Afula Israel

4. Hematology Division; Hadassah Medical Center; Jerusalem Israel

5. Hematology Department; Emek Medical Center; Afula Israel

6. Efrati Research Laboratory for Blood Cells and Cytology; Kaplan Medical Center; Rehovot Israel

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ejh.12694/fullpdf

Reference19 articles.

1. Hb Taybe (α 38 or 39 THR deleted): an α-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygous;Galacteros;C R Acad Sci III,1994

2. Hb Taybe (α38 or 39 Thr deleted): a new unstable α chain hemoglobin variant;Girodon;Blood [Suppl],1992

3. Hydrops fetalis associated with homozygosity for hemoglobin Taybe (α 38/39 THR deletion) in newborn triplets;Arnon;Am J Hematol,2004

4. Compound heterozygosity for two α-globin gene defects, Hb Taybe (α 1; 38 or 39 minus Thr) and a poly A mutation (α 2; AATAAA->AATAAG), results in a severe hemolytic anemia;Pobedimskaya;Am J Hematol,1994

5. HB Taybe: description of genetics and laboratory findings in an Israeli Arab family;Ben-Bassat;Hemoglobin,1998

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