A carregar...
Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders
BACKGROUND: Rare denovo variants represent a significant cause of neurodevelopmental delay and intellectual disability (ID). METHODS: Exome sequencing was performed on 4351 patients with global developmental delay, seizures, microcephaly, macrocephaly, motor delay, delayed speech and language develo...
Na minha lista:
| Publicado no: | J Neurodev Disord |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6593513/ https://ncbi.nlm.nih.gov/pubmed/31238879 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-019-9270-4 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|