Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism - Indian experience

Annals of Hematology

Volumn 82, Issue 7, 2003, Pages 427-430

  Chowdhury, M R ^a   Tiwari, M ^a   Kabra, M ^a   Menon, P S N ^a  

^a ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

Extragenic; Factor VIII; Intragenic; Polymorphism; Prenatal diagnosis

Indexed keywords

BLOOD CLOTTING FACTOR 8; ONCOPROTEIN; TYPE II SITE SPECIFIC DEOXYRIBONUCLEASE;

ARTICLE; CHORION VILLUS SAMPLING; CLINICAL ARTICLE; CONTROLLED STUDY; FAMILY HISTORY; FEMALE; GENETIC POLYMORPHISM; GENETIC SCREENING; HAPLOTYPE; HEMOPHILIA A; HETEROZYGOTE; HUMAN; INDIA; INTRON; LINKAGE ANALYSIS; MARKER GENE; MULTIGENE FAMILY; MUTATIONAL ANALYSIS; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; TANDEM REPEAT;

CHORIONIC VILLI; FACTOR VIII; FEMALE; HEMOPHILIA A; HUMANS; INDIA; LINKAGE (GENETICS); MALE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; PREDICTIVE VALUE OF TESTS; PREGNANCY; PRENATAL DIAGNOSIS; TANDEM REPEAT SEQUENCES;

EID: 0042133295     PISSN: 09395555     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00277-003-0670-9     Document Type: Article

References (14)

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