2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis

Chromosome 2q37 deletion syndrome is a rare chromosomal disorder characterized by mild to moderate developmental delay, brachydactyly of the third to fifth digits or toes, short stature, obesity, hypotonia, a characteristic facial appearance, and autism spectrum disorder. Here, we report on a patien...

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Detalles Bibliográficos
Autores principales: Cho, Eun-Kyung, Kim, Jinsup, Yang, Aram, Cho, Sung Yoon, Jin, Dong-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Endocrinology 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5495980/
https://www.ncbi.nlm.nih.gov/pubmed/28690993
http://dx.doi.org/10.6065/apem.2017.22.2.129

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5495980/
https://www.ncbi.nlm.nih.gov/pubmed/28690993
http://dx.doi.org/10.6065/apem.2017.22.2.129

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