Chromosome Deletion of 14q32.33 Detected by Array Comparative Genomic Hybridization in a Patient with Features of Dubowitz Syndrome

We report a 4-year-old girl of Mexican origins with a clinical diagnosis of Dubowitz syndrome who carries a de novo terminal deletion at the 14q32.33 locus identified by array comparative genomic hybridization (aCGH). Dubowitz syndrome is a rare condition characterized by a constellation of features...

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Detalles Bibliográficos
Autores principales: Darcy, Diana C., Rosenthal, Scott, Wallerstein, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447229/
https://www.ncbi.nlm.nih.gov/pubmed/23074674
http://dx.doi.org/10.1155/2011/306072

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447229/
https://www.ncbi.nlm.nih.gov/pubmed/23074674
http://dx.doi.org/10.1155/2011/306072

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