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Baraitser and Winter syndrome with growth hormone deficiency

Baraitser–Winter syndrome (BWS), first reported in 1988, is apparently due to genetic abnormalities that are still not well-defined, although many gene abnormalities are already discovered and de novo missense changes in the cytoplasmic actin-encoding genes (called ACTB and ACTG1) have been recently...

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Detalles Bibliográficos
Autores principales:	Chentli, Farida, Zellagui, Hadjer
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2014
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302548/ https://www.ncbi.nlm.nih.gov/pubmed/25624931 http://dx.doi.org/10.4103/1817-1745.147583

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