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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...
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| Publicado no: | BMC Med Genomics |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | 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 |
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