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Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34)

机译:Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34)

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摘要

Deficiency of coagulation factors VII and X was found in two patients (Erlangen and Nancy) who shared the same chromosomal aberration 46,XY,t(13;Y)(q11;q34) with probable loss of a terminal segment of 13q. Loci involved in synthesis or constitution of these factors may be located at 13 (q34).

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  • 来源
    《Human Genetics》 |1982年第4期|358-360|共页
  • 作者单位

    Institut für Humangenetik der Friedrich-Alexander-Universität Erlangen-Nürnberg;

    Universitäts-Kinderklinik;

    Centre Regional de Transfusion Sanguine et d'Hematologie de NancyCentre Regional de Transfusion Sanguine et d'Hematologie de Nancy;

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  • 正文语种 英语
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