Literature DB >> 11480787

Prenatal diagnosis of Hb H disease caused by a homozygosity for the alpha2 poly A (AATAAA-->AATAAG) mutation.

M A Cürük1, Y Kilinç, C Evrüke, F T Ozgünen, K Aksoy, G T Yüreğir.   

Abstract

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Year:  2001        PMID： 11480787     DOI： 10.1081/hem-100104034

Source DB:  PubMed          Journal:  Hemoglobin        ISSN： 0363-0269            Impact factor:   0.849


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  2 in total

1.  Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective.

Authors:  Zeynep Karakaş; Begüm Koç; Sonay Temurhan; Tuğba Elgün; Serap Karaman; Gamze Asker; Genco Gençay; Çetin Timur; Zeynep Yıldız Yıldırmak; Tiraje Celkan; Ömer Devecioğlu; Filiz Aydın
Journal:  Turk J Haematol       Date:  2015-08-06       Impact factor: 1.831

2.  Detection of Common Deletional of α-Thalassemia 3.7 Kb from Metropolitan Region of Manaus, Amazonas, Brazil.

Authors:  Fernanda Cozendey Anselmo; Abdou Gafar Soumanou; Cleidiane de Aguiar Ferreira; Flora Maia Viga Sobrinha; Ana Caroline Santos Castro; Rafael Oliveira Brito; Adolfo José da Mota; Marilda de Souza Gonçalves; José Pereira de Moura Neto
Journal:  Mediterr J Hematol Infect Dis       Date:  2021-01-01       Impact factor: 2.576
  2 in total

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