Mosaics and haemophilia

Haemophilia

Volumn 15, Issue 6, 2009, Pages 1181-1186

  Kasper, C ^a   Buzin, C H ^b  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b MEDomics   (United States)

Author keywords

Factor IX; Factor VIII; Haemophilia A; Haemophilia B; Mosaics; Mutation

Indexed keywords

BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9;

ANEUPLOIDY; AUTOSOMAL DOMINANT INHERITANCE; CHIMERA; CHROMOSOME ABERRATION; CPG ISLAND; DISEASE SEVERITY; DNA REPAIR; DUCHENNE MUSCULAR DYSTROPHY; EMBRYO CELL; EMBRYO DEVELOPMENT; GENE MUTATION; GENETIC PREDISPOSITION; GERM CELL; HEMOPHILIA A; HEMOPHILIA B; HETEROZYGOTE; HUMAN; KARYOTYPE; KARYOTYPE 46,XX; MOSAICISM; MUTATIONAL ANALYSIS; NONHUMAN; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SEX CHROMOSOMAL INHERITANCE; SOMATIC CELL; SPERMATOCYTE; SYMPTOM; TURNER SYNDROME; X CHROMOSOME INACTIVATION; X CHROMOSOME LINKAGE; Y CHROMOSOME;

CHIMERA; FEMALE; GENETIC DISEASES, X-LINKED; GENETIC PREDISPOSITION TO DISEASE; HEMOPHILIA A; HUMANS; MALE; MOSAICISM; PHENOTYPE; X CHROMOSOME INACTIVATION;

EID: 70449584757     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2009.02003.x     Document Type: Review

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