Inversion of intron 22 of the factor VIII gene in a girl with severe hemophilia A and Turner's syndrome [17]

Thrombosis and Haemostasis

Volumn 82, Issue 4, 1999, Pages 1379-

  Chuansumrit, A ^a   Sasanakul, W ^a   Goodeve, A ^a   Treratvirapong, T ^a   Parinayok, R ^a   Pintadit, P ^a   Hathirat, P ^a  

^a MAHIDOL UNIVERSITY   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 8; RISTOCETIN; VON WILLEBRAND FACTOR;

ADULT; BLEEDING DISORDER; BLOOD CLOTTING DISORDER; CAPILLARY RESISTANCE; CHILDHOOD DISEASE; CHROMOSOME INVERSION; DINUCLEOTIDE REPEAT; DISEASE SEVERITY; FATHER; FEMALE; GINGIVA BLEEDING; HEMARTHROSIS; HEMATOLOGY; HEMOPHILIA A; HETEROZYGOTE; HUMAN; HUMAN CELL; INTRON; KNEE INJURY; LETTER; LYMPHOCYTE CULTURE; MALE; MOTHER; PHYSICAL EXAMINATION; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SIBLING; SOUTHERN BLOTTING; TANDEM REPEAT; TURNER SYNDROME; X CHROMOSOMAL INHERITANCE; X CHROMOSOME ABERRATION;

EID: 0032828545     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1614406     Document Type: Letter

References (6)