Molecular Basis of A-Thalassa in Portugal-Reference-Cited by-同舟云学术

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Molecular Basis of A-Thalassa in Portugal

Published:1995-01 Issue:6 Volume:19 Page:343-352
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Peres M. J.,Romão L.,Carreiro H.,Picanço I.,Batalha L.,Magalhães H. A.,Martins M. C.,Lavinha J.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269509005826

Reference40 articles.

1. Localization of the human α-globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridization assay

2. Localisation of human alpha globin to 16p13.3----pter.

3. The chromosomal arrangement of human α-like globin genes: Sequence homology and α-globin gene deletions

4. A major positive regulatory region located far upstream of the human alpha-globin gene locus.

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1. Prevalence Rate of Thalassemia Carriers among Individuals with Microcytosis or Hypochromia in Portugal;Acta Médica Portuguesa;2023-03-10

2. Non–transfusion-dependent β-Thalassemia Because of a Single β-Thalassemia Mutation and Coinherited α-Globin Gene Triplication: Need for Increased Awareness to Prevent Incorrect and Delayed Diagnosis;Journal of Pediatric Hematology/Oncology;2019-04-08

3. The Frequency of α-Globin Gene Triplication in a Southern Chinese Population;Indian Journal of Hematology and Blood Transfusion;2015-09-02

4. Frequency and spectrum of hemoglobinopathy mutations in a Uruguayan pediatric population;Genetics and Molecular Biology;2013-07-19

5. Hb Plasencia [α125(H8)Leu→Arg (α2)] is a Frequent Cause ofα+-Thalassemia in the Portuguese Population;Hemoglobin;2013-01-31

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