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pro vyhledávání: '"Suha Mustafa Hassan"'
Autor:
Suha Mustafa Hassan, Muhanna Al Muslahi, Muna Al Riyami, Abeer Al Balushi, Egbert Bakker, Cornelis L. Harteveld, Piero C. Giordano
Publikováno v:
Thalassemia Reports, Vol 5, Iss 1 (2015)
Despite the fact that patients homozygous for the sickle cell disease (SCD) mutation have an identical genotype, the severity of the disease can be extremely variable. The hemoglobin (Hb) S mutation has been described on five different haplotypes wit
Externí odkaz:
https://doaj.org/article/f1dd7f20447c4c358b4187dba84d9118
Publikováno v:
Thalassemia Reports, Vol 4, Iss 1 (2014)
Hemoglobinopathies (HBP) are the most common genetic disorder in Oman and are in need of prevention programs due to the high incidence of β-thalassemia major and sickle cell disease. Prenatal diagnosis (PD) and selective pregnancy termination is sho
Externí odkaz:
https://doaj.org/article/0da9f7d84789439285f50c7ef1d4a579
Publikováno v:
BMJ Case Reports. 16:e254416
Beta-thalassaemia is one of the most common genetic disorders worldwide, which is caused by absent or decreased synthesis of beta-globin chain subunits. Beta-thalassaemias are diverse groups of disease with a wide spectrum of clinical phenotypes. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::133d3841e77092d947dce569d8e1b9be
https://doi.org/10.1136/bcr-2022-254416
https://doi.org/10.1136/bcr-2022-254416