Deletion of the factor IX gene as a result of translocation t(X;1) in a girl affected by haemophilia B

British Journal of Haematology

Volumn 113, Issue 3, 2001, Pages 616-620

  Krepischi Santos, A C V ^a   Carneiro, J D A ^a   Svartman, M ^a   Bendit, I ^b   Odone Filho, V ^a   Vianna Morgante, Angela M ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b FUNDAÇÃO PRÓ SANGUE HEMOCENTRO DE SÃO PAULO   (Brazil)

Author keywords

Chromosome X; Factor IX gene; Haemophilia B; X inactivation; X; autosome translocation

Indexed keywords

BLOOD CLOTTING FACTOR 9; DNA;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION X; CYTOLOGY; DISEASE SEVERITY; DNA DETERMINATION; DNA METHYLATION; FEMALE; GENE DELETION; GENE INACTIVATION; HEMOPHILIA B; HUMAN; PATHOGENESIS; PRIORITY JOURNAL; SCHOOL CHILD;

EID: 0034993219     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2001.02786.x     Document Type: Article

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