Extended Molecular Spectrum of β- and α-Thalassemia in Oman-Reference-Cited by-同舟云学术

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Extended Molecular Spectrum of β- and α-Thalassemia in Oman

Published:2010-03-30 Issue:2 Volume:34 Page:127-134
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Hassan Suha M.,Hamza Nishat,Jaffer Al-Lawatiya Fatma,Jaffer Mohammed Ali,Harteveld Cornelis L.,Rajab Anna,Giordano Piero C.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630261003673147

Reference11 articles.

1. Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populations

2. A simple salting out procedure for extracting DNA from human nucleated cells

3. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions

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1. Homozygous mild beta-thalassaemia promoter transversion −71 C>T HBB:c.-121 C>T;BMJ Case Reports;2023-04

2. Genetic variation patterns of β-thalassemia in Western Andalusia (Spain) reveal a structure of specific mutations within the Iberian Peninsula;Annals of Human Biology;2021-07-04

3. The worldwide molecular spectrum and distribution of thalassaemia: a systematic review;Annals of Human Biology;2021-05-19

4. The spectrum of beta-thalassemia mutations in the 22 Arab countries: a systematic review;Expert Review of Hematology;2020-12-29

5. Frequency and genotyping of alpha thalassemia in individuals undergoing premarital screening;Journal of the Pakistan Medical Association;2020-10-05

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