Rett Syndrome in a Boy with a 47,XXY Karyotype

Author:

Salomão Schwartzman José,Zatz Mayana,dos Reis Vasquez Luciana,Ribeiro Gomes Raquel,Koiffmann Célia P.,Fridman Cintia,Guimarães Otto Priscilla

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference43 articles.

1. Rett-like syndrome in fragile X syndrome;Alembick;Genet Couns,1995

2. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation;Allen;Am J Hum Genet,1992

3. Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations;Archidiacono;Hum Genet,1991

4. X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probe;Camus;Hum Genet,1996

5. Male Rett variant;Christen;Neuropediatrics,1995

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