First report of the spectrum of δ-globin gene mutations in Omani subjects - identification of novel mutations-Reference-Cited by-同舟云学术

First report of the spectrum of δ-globin gene mutations in Omani subjects - identification of novel mutations

Published:2014-07-09 Issue:2 Volume:37 Page:238-243
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int. Jnl. Lab. Hem.

Author:

Alkindi S.¹,AlZadjali S.²,Daar S.¹,Ambusaidi R.²,Gravell D.²,Al Haddabi H.²,Krishnamoorthy R.³⁴,Pathare A.²

Affiliation:

1. College of Medicine & Health Sciences; Sultan Qaboos University; Muscat Oman

2. Sultan Qaboos University Hospital; Muscat Oman

3. INSERM, U665; Paris France

4. Laboratoire d'Excellence GR-EX; Paris France

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Reference20 articles.

1. A community-based study of common hereditary blood disorders in Oman;Al-Riyami;East Mediterr Health J,2001

2. Forecasting hemoglobinopathy burden through neonatal screening in Omani neonates;Alkindi;Hemoglobin,2010

3. Newborn hemoglobinopathy carrier screening: towards comprehensive and improved patient care of sickle cell disease in Oman, a cost effective analysis (Abstr. 806);Pathare;Hematol J,2006

4. Severity ranking of non-deletional alpha thalassemic alleles: insights from an Omani family study;Wali;Eur J Haematol,2011

5. A stepwise α thalassemia screening strategy in high prevalence areas;Alkindi;Eur J Haematol,2013

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