Cytogenetic and molecular contributions to the study of mental retardation

Author:

Llerena Jr. Juan C.1,Almeida José Carlos Cabral de1

Affiliation:

1. FIOCRUZ

Publisher

FapUNIFESP (SciELO)

Subject

Genetics,Molecular Biology

Reference37 articles.

1. Tandem duplication of 11p12-p13 in a child with borderline development delay and eye abnormalities: dose effect of the PAX6 gene product?;Aalfs C.M.;Am. J. Med. Genet.,1997

2. Pyruvate dehydrogenase deficiency;Brown G.K.;J. Med. Genet.,1994

3. A complex chromosomal rearrangement with at least 9 breakpoints in a mentally retarded boy characterized by FISH;Cabral de Almeida J.C.;Am. J. Hum. Genet.,1997

4. FISH studies in a patient with sporadic aniridia and t(7;11)(q.312;p13);Crolla J.A.;J. Med. Genet.,1996

5. Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype;Erdel M.;Hum. Genet.,1997

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