Noonan syndrome – a new survey

Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genetic features. Various symptoms have been reported for this abnormality such as short stature, unusual facial characteristics, congenital heart abnormalities, developmental complications, and an elevate...

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Detalles Bibliográficos
Autores principales: Tafazoli, Alireza, Eshraghi, Peyman, Koleti, Zahra Kamel, Abbaszadegan, Mohammadreza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2016
Materias:
State of the Art Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206377/
https://www.ncbi.nlm.nih.gov/pubmed/28144274
http://dx.doi.org/10.5114/aoms.2017.64720

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206377/
https://www.ncbi.nlm.nih.gov/pubmed/28144274
http://dx.doi.org/10.5114/aoms.2017.64720

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