Familial inheritance of the 3q29 microdeletion syndrome: case report and review
Abstract 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...
Furkejuvvon:
| Váldodahkkit: | , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
BMC
2019-03-01
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| Ráidu: | BMC Medical Genomics |
| Fáttát: | |
| Liŋkkat: | http://link.springer.com/article/10.1186/s12920-019-0497-4 |
| Fáddágilkorat: |
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