The clinical severity of hemoglobin S/Black (A γδβ)0 -thalassemia-Reference-Cited by-同舟云学术

The clinical severity of hemoglobin S/Black (A γδβ)0 -thalassemia

Published:2017-04-28 Issue:11 Volume:64 Page:e26596
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Cancio Maria I.¹,Aygun Banu²,Chui David H. K.³,Rothman Jennifer A.⁴,Scott J. Paul⁵,Estepp Jeremie H.⁶,Hankins Jane S.⁶

Affiliation:

1. Department of Pediatrics; Memorial Sloan Kettering Cancer Center; New York New York

2. Cohen Children's Medical Center of New York; New Hyde Park New York

3. Hemoglobin Diagnostic Reference Laboratory; Departments of Medicine; Pathology and Laboratory Medicine; Boston Medical Center; Boston Massachusetts

4. Department of Pediatrics; Duke University Medical Center; Durham North Carolina

5. Department of Pediatrics; Medical College of Wisconsin; Blood Research Institute; Children's Research Institute; Milwaukee Wisconsin

6. Department of Hematology; St. Jude Children's Research Hospital; Memphis Tennessee

Funder

National Cancer Institute

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference6 articles.

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2. (A gamma delta beta)0-Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA;Henthorn;Br J Haematol,1985

3. Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin;Ngo;Br J Haematol,2012

4. Clinical and molecular characterization of beta(S) and (G)gamma((A)gammadeltabeta)(0)-thalassemia in eastern India;Patel;Hemoglobin,2010

5. Fetal hemoglobin in sickle cell anemia: a glass half full?;Steinberg;Blood,2014

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2. Clinical phenotypes of three children with sickle cell disease caused by HbS /Sicilian (δβ) ⁰ ‐thalassemia deletion;American Journal of Hematology;2022-01-26

3. Sickle cell haemoglobin and its interactions with other variant haemoglobins and with thalassaemias;Haemoglobinopathy Diagnosis;2020-02-28

4. HbS-Sicilian (δβ)0-Thalassemia: A Rare Variant of Sickle Cell;Case Reports in Hematology;2017