Familial deletion 18p syndrome: case report

BACKGROUND: Deletion 18p is a frequent deletion syndrome characterized by dysmorphic features, growth deficiencies, and mental retardation with a poorer verbal performance. Until now, five families have been described with limited clinical description. We report transmission of deletion 18p from a m...

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Detalles Bibliográficos
Autores principales: Maranda, Bruno, Lemieux, Nicole, Lemyre, Emmanuelle
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1540411/
https://www.ncbi.nlm.nih.gov/pubmed/16842614
http://dx.doi.org/10.1186/1471-2350-7-60

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1540411/
https://www.ncbi.nlm.nih.gov/pubmed/16842614
http://dx.doi.org/10.1186/1471-2350-7-60

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