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Linkage studies in a large fragile X family.
Patterson, M; Bell, M; Kress, W; Davies, K E; Froster-Iskenius, U.
Afiliación
  • Patterson M; Nuffield Department of Clinical Medicine, John Radcliffe Hospital, Oxford, England.
Am J Hum Genet ; 43(5): 684-8, 1988 Nov.
Article en En | MEDLINE | ID: mdl-2903666
ABSTRACT
We have analyzed the segregation of five loci in the region Xq27/28 in a large family affected by the fragile X syndrome. The marker DXS115 (767) is shown to be polymorphic with the enzyme PstI, as well as with BstXI. This marker will be useful in the analysis of both fragile X and haemophilia A families. The data presented here are consistent with the following order of loci Xcen-F9-DXS105(cX55.7,55E)-DXS98(4D-8)- FRAXA-DXS52(St14)-DXS115(767)-qter.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aberraciones Cromosómicas Sexuales / Síndrome del Cromosoma X Frágil / Ligamiento Genético Límite: Female / Humans / Male Idioma: En Revista: Am J Hum Genet Año: 1988 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aberraciones Cromosómicas Sexuales / Síndrome del Cromosoma X Frágil / Ligamiento Genético Límite: Female / Humans / Male Idioma: En Revista: Am J Hum Genet Año: 1988 Tipo del documento: Article País de afiliación: Reino Unido
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