Fragile X syndrome in a normal IQ male with learning and emotional problems.
A case study is presented of an adult male who was diagnosed with fragile X syndrome after the identification of this syndrome in his more affected brother. Fragile X syndrome is the principal inherited cause of mental retardation and stems from a trinucleotide repeat mutation in the FMR1 gene, lea...
| Publicado en: | Journal of the American Academy of Child & Adolescent Psychiatry Vol. 33; pp. 1316 - 1322 |
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| Autores principales: | , , |
| Formato: | Artículo |
| Publicado: |
Elsevier Science
November/December 1994
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| Materias: | |
| Acceso en línea: | Ver este registro en EBSCOhost |