Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome

Recurrent deletions of 2q32q33 have recently been reported as a new microdeletion syndrome. Clinical features of this syndrome include severe mental retardation, growth retardation, dysmorphic features, thin and sparse hair, feeding difficulties and cleft or high palate. The commonly deleted region...

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Detalles Bibliográficos
Autores principales: Rosenfeld, Jill A., Ballif, Blake C., Lucas, Ann, Spence, Edward J., Powell, Cynthia, Aylsworth, Arthur S., Torchia, Beth A., Shaffer, Lisa G.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2719055/
https://www.ncbi.nlm.nih.gov/pubmed/19668335
http://dx.doi.org/10.1371/journal.pone.0006568

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2719055/
https://www.ncbi.nlm.nih.gov/pubmed/19668335
http://dx.doi.org/10.1371/journal.pone.0006568

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