Výsledky vyhledávání - "Ebtihal Salman"

Various α-Thalassemia Genotype Combinations of the Saudi-Type Polyadenylation Signal Mutation (αT-Saudiα) in the Population of Bahrain: An Update of Genotype-Phenotype Analyses

Autor: Ahmed Thabet, Nabeel J. Al Moamen, Ebtihal Salman, Fawzia Mahdi, Hema Newton

Publikováno v: Hemoglobin. 42:166-170

The Saudi-type polyadenylation (polyA) signal mutation on the α2-globin gene, HBA2: c.*94A > G; AATAAA>AATAAG; αT-Saudiα, is one of the major α-thalassemia (α-thal) determinants in the population o...

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a4df568f8ab7030299101bcc62c56720
https://doi.org/10.1080/03630269.2018.1499523

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Various α-Thalassemia Genotype Combinations of the Saudi-Type Polyadenylation Signal Mutation (α

Autor: Nabeel J, Al Moamen, Ahmed, Thabet, Fawzia, Mahdi, Hema, Newton, Ebtihal, Salman

Publikováno v: Hemoglobin. 42(3)

The Saudi-type polyadenylation (polyA) signal mutation on the α2-globin gene, HBA2: c.*94A G; AATAAAAATAAG; α

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c08e590385f21412a0e4082d933e63b9
https://pubmed.ncbi.nlm.nih.gov/30864492

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Silent β-Thalassemia Mutations at −101 (C>T) and −71 (C>T) and Their Coinheritance with the Sickle Cell Mutation in Bahrain

Autor: Al Alawi Ahmed, Thabet Ahmed, Nabeel J. Al Moamen, Hassan Sanad, Shaikha Al Arrayed, Ruqaya Abbas, Fawzia Mahdi, Ebtihal Salman

Publikováno v: Hemoglobin. 37:369-377

Silent β-thalassemia (β-thal) is a group of mutations affecting the β-globin gene that cannot be differentiated in heterozygote states from normal conditions by using conventional criteria for the diagnosis of β-thal trait. Here we report the exi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5f8d1752025235103d2aeb9e9010a67
https://doi.org/10.3109/03630269.2013.785434

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Diverse Genotype Presentation of the Saudi-Type Polya Signal Mutation (αTsaudiα) in the Population of Bahrain

Autor: Rugaya Abbas, Fawzia Mahdi, Nabeel J. Al Moamen, Ebtihal Salman, Ahmed Al Alawi, Ahmed Thabet

Publikováno v: International Journal of Blood Research and Disorders. 2

TSaudi α) haplotype in our population and their relevant phenotypes. A total of 1187 patients with α-thalassemia phenotype presentation have been recruited for this investigation. Preliminary diagnosis of α-thalassemia was based on low hematologic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::695a6d24b7e0f4da85497e3a84561ef5
https://doi.org/10.23937/2469-5696/1410004

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