St 14 (DX S52) VNTR polymorphism in the Indian population and its application in carrier detection and prenatal diagnosis of haemophilia A families

Haematologia

Volumn 30, Issue 3, 2000, Pages 203-207

  Shetty, S ^a   Ghosh, K ^a   Mohanty, D ^a  

^a KEM HOSPITAL   (India)

Author keywords

Haemophilia A; Polymorphism; St 14 allele frequency

Indexed keywords

BLOOD CLOTTING FACTOR 8;

ALLELE; ARTICLE; FEMALE; GENETIC POLYMORPHISM; GENETICS; HEMOPHILIA A; HETEROZYGOTE; HUMAN; INDIA; MALE; PRENATAL DIAGNOSIS; VARIABLE NUMBER OF TANDEM REPEAT;

ALLELES; FACTOR VIII; FEMALE; HEMOPHILIA A; HETEROZYGOTE; HUMANS; INDIA; MALE; MINISATELLITE REPEATS; POLYMORPHISM, GENETIC; PRENATAL DIAGNOSIS;

EID: 0033641921     PISSN: 00176559     EISSN: None     Source Type: Journal    
DOI: 10.1163/156855900300109206     Document Type: Article

References (6)

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