Loading...
Familial inheritance of the 3q29 microdeletion syndrome: case report and review
BACKGROUND: The chromosome 3q29 microdeletion syndrome is characterized by a clinical phenotype that includes behavioral features consistent with autism and attention deficit hyperactivity disorder, mild to moderate developmental delay, language-based learning disabilities, and/or dysmorphic feature...
Na minha lista:
| Udgivet i: | BMC Med Genomics |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2019
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6421695/ https://ncbi.nlm.nih.gov/pubmed/30885185 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-019-0497-4 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|