BRIEF REPORT: AUTISM OF THE ASPERGER TYPE ASSOCIATED WITH AN AUTOSOMAL FRAGILE SITE

Antzeko izenburuak

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• MENDELIAN INHERITANCE IN MAN. CATALOGS OF AUTOSOMAL DOMINANT, AUTOSOMAL RECESSIVE, AND X-LINKED PHENOTYPES, 6 ED.
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• Síndrome de Prader-Willi por disomia uniparental materna y un cariotipo con un cromosoma marcador en mosaico
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• Síndrome X Frágil
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