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Br J Haematol ; 29(2): 319-28, 1975 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-1191552

RESUMO

A large kindred with combined deficiencies of factors VII and IX is presented. The deficiencies appeared to be independent and the data were not consistent with a diagnosis of haemophilia BM. The identification of mildly affected family members, including carriers of haemophilia B and heterozygotes for factor-VII deficiency, was facilitated by comparison with the 95% confidence interval of an age- and sex-matched control population. The bleeding patterns were those of mild to moderate haemophilia B and did not appear to have been modified by the presence of factor-VII deficiency.


Assuntos
Deficiência do Fator VII/sangue , Hemofilia B/sangue , Fator IX/análise , Fator VII/análise , Deficiência do Fator VII/complicações , Deficiência do Fator VII/genética , Hemofilia B/complicações , Hemofilia B/genética , Humanos , Masculino , Pessoa de Meia-Idade , Linhagem , Protrombina/análise , Tromboplastina/análise
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