A MULTI-CENTER STUDY IN ORDER TO FURTHER DEFINE THE MOLECULAR BASIS OF β-THALASSEMIA IN THAILAND, PAKISTAN, SRI LANKA, MAURITIUS, SYRIA, AND INDIA, AND TO DEVELOP A SIMPLE MOLECULAR DIAGNOSTIC STRATEGY BY AMPLIFICATION REFRACTORY MUTATION SYSTEM-POLYMERASE CHAIN REACTION-Reference-Cited by-同舟云学术

A MULTI-CENTER STUDY IN ORDER TO FURTHER DEFINE THE MOLECULAR BASIS OF β-THALASSEMIA IN THAILAND, PAKISTAN, SRI LANKA, MAURITIUS, SYRIA, AND INDIA, AND TO DEVELOP A SIMPLE MOLECULAR DIAGNOSTIC STRATEGY BY AMPLIFICATION REFRACTORY MUTATION SYSTEM-POLYMERASE CHAIN REACTION

Published:2001-01 Issue:4 Volume:25 Page:397-407
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Old John M.,Khan Shaheen N.,Verma Ishwar,Fucharoen Suthat,Kleanthous Marina,Ioannou Panos,Kotea Navaratnam,Fisher Christopher,Riazuddin Sheikh,Saxena Renu,Winichagoon Pranee,Kyriacou Kyriacos,Al-Quobaili Faizeh,Khan Baldip

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.1081/HEM-100107877

Reference21 articles.

1. Prenatal screening for haemoglobin disorders

2. Hemoglobinopathies: Community Clues to Mutation Detection

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