Prevalence of sporadic and familial haemophilia

Haemophilia

Volumn 13, Issue 1, 2007, Pages 90-92

  Kasper, Carol K ^a,b   Lin, J C ^a,c  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b Brigham and Women's Hospital ^*  (United States)

^c BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

Hemophilia A; Hemophilia B; Hemophilia inheritance

Indexed keywords

ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; FAMILIAL DISEASE; FEMALE; GENE MUTATION; GRANDPARENT; HEMOPHILIA A; HEMOPHILIA B; HUMAN; LEUKOCYTE; MAJOR CLINICAL STUDY; MALE; MOTHER; PEDIGREE ANALYSIS; PREVALENCE; PRIORITY JOURNAL; PROGENOTE; RETROSPECTIVE STUDY; SIBLING;

CALIFORNIA; CARRIER STATE; FEMALE; HEMOPHILIA A; HEMOPHILIA B; HUMANS; MALE; MOSAICISM; MUTATION; PEDIGREE; PREVALENCE; RETROSPECTIVE STUDIES;

EID: 33845773426     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2006.01397.x     Document Type: Article

References (4)

1. Biggs R, Macfarlane, RG. Treatment of Haemophilia and other Coagulation Disorders. Philadelphia: F.A. Davis Company, 1966; 22.
2. Biggs R, Rizza CR. The sporadic case of haemophilia A. Lancet 1976; 7982: 431-433.
3. Strauss HS. The perpetuation of hemophilia by mutation. Pediatrics 1967; 39: 186-193.
4. Francis RB Jr, Kasper CK. Reproduction in hemophilia. JAMA 1983; 250: 3192-3195.