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Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysis.
Hamel, B C; Smits, A P; van den Helm, B; Smeets, D F; Knoers, N V; van Roosmalen, T; Thoonen, G H; Assman-Hulsmans, C F; Ropers, H H; Mariman, E C; Kremer, H.
Afiliación
  • Hamel BC; Department of Human Genetics, University Hospital, Nijmegen, The Netherlands. b.hamel@antrg.azn.nl
Am J Med Genet ; 85(3): 290-304, 1999 Jul 30.
Article en En | MEDLINE | ID: mdl-10398246
ABSTRACT
Four families are described in which mental retardation segregates in an X-linked fashion. Mental retardation was the only consistent clinical finding in all affected males. The degree of retardation varied from mild to profound both between and within families. Linkage analysis localized the genetic defect of MRX43 to Xp22. 31-p21.2, MRX44 to Xp11.3-p11.21, MRX45 to Xp11.3-p11.21, and MRX52 to Xp11.21-q21.33 with LOD scores of >2 at straight theta = 0.0 in all four families.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromosoma X / Discapacidad Intelectual Tipo de estudio: Observational_studies / Prognostic_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Med Genet Año: 1999 Tipo del documento: Article País de afiliación: Países Bajos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromosoma X / Discapacidad Intelectual Tipo de estudio: Observational_studies / Prognostic_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Med Genet Año: 1999 Tipo del documento: Article País de afiliación: Países Bajos
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