| Document Date: 2014-01-10 15:42:26
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Company VWD / / Country Pakistan / India / / MedicalCondition mutant gene causing hemophilia / Common recessive singlegene disorders / muscular dystrophy / mild protein deficiency / hemophilia A / autosomal dominant disorders / Severe hemophilia / mild and moderate hemophilia A / mild hemophilia / hemophilia B / autosomal recessive bleeding disorders / VIII deficiency / diabetes / neurofibromatosis / severe hemophilia B / 2M von Willebrand disease / immune deficiency / genetic hyperlipidemias / disorder / autosomal recessive disorders / sickle cell disease / von Willebrand disease / osteogenesis imperfecta / genetic clotting disorders / cystic fibrosis / Turner‘s syndrome / familial hemophilia / IX deficiency / hemophilia / color blindness / severe hemophilia A / disorders / sporadic hemophilia / Klinefelter‘s syndrome / / MedicalTreatment counseling / / Person AGA AGG AGC AGT / Carol K. Kasper / Carolyn H. Buzin / / Position nurse / physician / messenger / / Product pseudo / glycine / / Region Near East / North Africa / / Technology recombination / CAT / ATG / /
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Genetics of Hemophilia A and B an Introduction for Clinicians, 2009