Human α‐Thalassemia syndromes: Detection of molecular defects-Reference-Cited by-同舟云学术

Human α‐Thalassemia syndromes: Detection of molecular defects

Published:1996-10 Issue:2 Volume:53 Page:81-91
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:American J Hematol

Author:

Kattamis Antonios C.¹,Camaschella Clara²,Sivera Piera²,Surrey Saul¹,Fortina Paolo¹

Affiliation:

1. Division of Hematology, Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania

2. Dipartimento di Scienze Biomediche ed Oncologia Umana, Sezione Clinica, Università degli Studi, CNR‐CIOS, Torino, Italy

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/%28SICI%291096-8652%28199610%2953%3A2%3C81%3A%3AAID-AJH5%3E3.0.CO%3B2-%23

Reference89 articles.

1. A review of the molecular genetics of the human α‐globin gene cluster;Higgs DR;Blood,1989

2. Locus assignment of human a globin mutations by selective amplification and direct sequencing

3. Rapid diagnosis of α‐thalassemia‐1 of Southeast Asia type, and hydrops fetalis by polymerase chain reaction;Chang J‐G;Blood,1991

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