טוען...
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...
שמור ב:
| הוצא לאור ב: | BMC Med Genomics |
|---|---|
| Main Authors: | , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2019
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| נושאים: | |
| גישה מקוונת: | 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 |
| תגים: |
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