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Possible intrachromosomal duplication in a case of trisomy 9p.
Hum Genet ; 34(2): 217-21, 1976 Oct 28.
Article en En | MEDLINE | ID: mdl-1002145
A 5-year-old boy with multiple minor anomalies and mental retardation was found to have chromosomal condition of 46,XY,inv dup(9p) (pter leads to p13::p21 leads to p24::p13 leads to qter). The clinical features of the propositus fit well with those of trisomy 9p which have been established to be a clinical entity.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trisomía / Cromosomas Humanos 6-12 y X Límite: Child, preschool / Humans / Male Idioma: En Revista: Hum Genet Año: 1976 Tipo del documento: Article Pais de publicación: Alemania
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trisomía / Cromosomas Humanos 6-12 y X Límite: Child, preschool / Humans / Male Idioma: En Revista: Hum Genet Año: 1976 Tipo del documento: Article Pais de publicación: Alemania