Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay

PURPOSE: The 1p36 deletion syndrome is a microdeletion syndrome characterized by developmental delays/intellectual disability, craniofacial dysmorphism, and other congenital anomalies. To date, many cases of this syndrome have been reported worldwide. However, cases with this syndrome have not been...

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Detalles Bibliográficos
Autores principales: Seo, Go Hun, Kim, Ja Hye, Cho, Ja Hyang, Kim, Gu-Hwan, Seo, Eul-Ju, Lee, Beom Hee, Choi, Jin-Ho, Yoo, Han-Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753195/
https://www.ncbi.nlm.nih.gov/pubmed/26893599
http://dx.doi.org/10.3345/kjp.2016.59.1.16

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753195/
https://www.ncbi.nlm.nih.gov/pubmed/26893599
http://dx.doi.org/10.3345/kjp.2016.59.1.16

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