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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.
Affiliation
  • 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 de 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.
Sujet(s)
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Chromosome X / Déficience intellectuelle Type d'étude: Observational_studies / Prognostic_studies Limites: Adult / Aged / Female / Humans / Male / Middle aged Langue: En Journal: Am J Med Genet Année: 1999 Type de document: Article Pays d'affiliation: Pays-Bas
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Chromosome X / Déficience intellectuelle Type d'étude: Observational_studies / Prognostic_studies Limites: Adult / Aged / Female / Humans / Male / Middle aged Langue: En Journal: Am J Med Genet Année: 1999 Type de document: Article Pays d'affiliation: Pays-Bas
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