Fragile X syndrome: clinical and cytogenetic studies

Three families with the fragile X syndrome were studied with the aim to establish the most frequent clinical signs in the affected individuals and heterozygous women. The clinical evaluation, IQ level measurements and cytogenetic studies were performed in 40 subjects, 20 males and 20 females. The fr...

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Bibliographic Details
Main Authors: TÊMIS MARIA FÉLIX, JOÃO MONTEIRO DE PINA-NETO
Format: Article
Language:English
Published: Academia Brasileira de Neurologia (ABNEURO) 1998-03-01
Series:Arquivos de Neuro-Psiquiatria
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1998000100002&tlng=en