Hemoglobin F Only Syndrome at Birth-Reference-Cited by-同舟云学术

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Hemoglobin F Only Syndrome at Birth

Published:2016-01 Issue:1 Volume:38 Page:e32-e34
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:

Author:

Yee Marianne E. M.,Quarmyne Maa-Ohui,Segbefia Catherine,Young Andrew N.,Zhuang Lina,Kutlar Ferdane

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference14 articles.

1. Diagnostic approach to hemoglobinopathies.;Kutlar;Hemoglobin,2007

2. . Diagnostic complication and molecular characteristics of Hb SC-Chicago disease with alpha-thal-2 (-alpha3.7 deletion): effects of multiple variant on patients phenotype.;Hughes;Ann Hematol,2009

3. . Molecular characterization of Hb D-Ibadan beta87(F3)Thr--Lys in combination with Hb S beta6(A3)Glu--Val and with beta-thalassemia: report of two cases.;Redding-Lallinger;Hemoglobin,2002

4. . Thalassemia-like phenotype in a novel complex hemoglobinopathy with alpha, beta, delta globin chain abnormalities.;Sabio;J Pediatr Hematol Oncol,2011

5. . Origin of Hb A2 (Hb B2) delta16(A13)Gly -- Arg (GGC -- CGC).;Bennani;Hemoglobin,2003

Cited by 2 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. A Case Report of Compound Heterozygosity for β0/β+-Thalassemia Resulting from under Diagnosed β-Thalassemia Found in a Hb A'2Sample;Hemoglobin;2019-01-02

2. A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)];Hemoglobin;2016-04-27

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