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در حال نمایش آیتم1-3 از 3

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?-thalassemia mutations in the iranian kurdish population of kurdistan and west azerbaijan provinces 

Haghi, M; Khorshidi, S; Feizi, MAH; Pouladi, N; HosseinpourFeizi, AA (2009)
The aim of this study was to investigate the prevalence and spectrum of ?-thalassemia (?-thal) mutations in the population of Sunni Muslim Kurds in western Iran and to set up a prenatal diagnostic laboratory. Sixty unrelated ...
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Homozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family 

Haghi, M; Hosseinpour Feizi, AA; Harteveld, CL; Pouladi, N; Hosseinpour Feizi, MA (2009)
The severity of ?-thalassemia (?-thal) is remarkable for its variability in different populations, even in different patients. We studied a family from Azerbaijan Province, Northwestern Iran, who had a rare ?0-thal mutation, ...
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Molecular spectrum of ?-thalassemia mutations in Northwestern Iran 

Hosseinpour Feizi, MA; Hosseinpour Feizi, AA; Pouladi, N; Haghi, M; Azarfam, P (2008)
?-Thalassemia (?-thal) is a hereditary autosomal disorder with decreased or absent ?-globin chain synthesis. This study was designed to identify the common and rare ?-thal mutations in the Azerbaijan provinces, Northwestern ...

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نویسنده
Haghi, M (3)
Pouladi, N (3)Hosseinpour Feizi, AA (2)Hosseinpour Feizi, MA (2)Azarfam, P (1)Feizi, MAH (1)Harteveld, CL (1)HosseinpourFeizi, AA (1)Khorshidi, S (1)موضوع
article (3)
beta thalassemia (3)beta-Thalassemia (3)
female (3)
frameshift mutation (3)human (3)
Humans (3)
Iran (3)
male (3)adolescent (2)... View MoreDate Issued2009 (2)2008 (1)Has File(s)
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مخزن دانش دانشگاه علوم پزشکی تبریز در نرم افزار دی اسپیس، کپی رایت 2018 ©  
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