HBB loss of heterozygosity in the hemopoietic lineage gives rise to an unusual sickle-cell trait phenotype.
نویسندگان
چکیده
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منابع مشابه
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OBJECTIVE To estimate the additional number of affected individuals based on the prevalence of sickle-cell syndromes among relatives of index cases. METHODS Cross-sectional study of relatives of a random sample of index cases identified through a neonatal screening program in Northeastern Brazil, between 2001 and 2005. The extended family trial model included 463 relatives of 21 index cases. ...
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ورودعنوان ژورنال:
- Haematologica
دوره 98 1 شماره
صفحات -
تاریخ انتشار 2013