A carregar...
A 15q14 microdeletion involving MEIS2 identified in a patient with autism spectrum disorder
We describe a 9-year-old male patient with a 15q14 microdeletion including MEIS2. The patient was born with a ventricular septal defect and submucosal cleft. Mild developmental disability and autism spectrum disorder diagnosed in childhood were also considered to be consequences of MEIS2 haploinsuff...
Na minha lista:
| Publicado no: | Hum Genome Var |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2017
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5517666/ https://ncbi.nlm.nih.gov/pubmed/28736618 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/hgv.2017.29 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|