Hemophilia B in a female

Acta Haematologica

Volumn 106, Issue 3, 2001, Pages 115-117

  Shetty, Shrimati ^a   Ghosh, Kanjaksha ^a   Mohanty, Dipika ^a  

^a KEM HOSPITAL   (India)

Author keywords

Female hemophilia; Hemophilia B; Polymorphism

Indexed keywords

BLOOD CLOTTING FACTOR 9; BLOOD CLOTTING FACTOR 9 COMPLEX; DNA; SILVER;

ALLELE; ARTICLE; BLOOD LEVEL; CASE REPORT; CLINICAL FEATURE; DISEASE SEVERITY; DNA POLYMORPHISM; FAMILY STUDY; FEMALE; GENE MUTATION; HEMOPHILIA B; HEREDITY; HETEROZYGOTE; HUMAN; KARYOTYPE 46,XX; MARKER GENE; PRIORITY JOURNAL; SCHOOL CHILD; SEGREGATION ANALYSIS; SEX LIMITATION; SYMPTOM; TURNER SYNDROME;

CHILD; FACTOR IX; FEMALE; GENOTYPE; HEMOPHILIA B; HUMANS; PEDIGREE; X CHROMOSOME;

EID: 0035174855     PISSN: 00015792     EISSN: None     Source Type: Journal    
DOI: 10.1159/000046599     Document Type: Article

References (9)

1. Female haemophilia A in a family with seeming extreme bidirectional lyonization tendency: Abnormal premature X-chromosome inactivation?
2. Hemophilia B in a 46,XX female probably caused by non-random X inactivation
3. Concomitant Turner syndrome and hemophilia A in a female with an idic(X)(p11) heterozygous at locus DXS52
4. A de novo translocation 46,Xt(X;15) causing haemophilia B in a girl: A case report
5. Hemophilia 'A' in a 46,X,i(Xq) female
6. Severe factor VIII and factor IX deficiency in females
7. Moderate haemophilia B in a female carrier caused by preferential inactivation of the paternal X chromosome
8. Report of a joint WHO/WFH meeting on the control of haemophilia: Carrier detection and prenatal diagnosis