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A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes
BACKGROUND: Most studies relative to Y chromosome abnormalities are focused on the sexual developmental disorders. Recently, a few studies suggest that some genes located on Y chromosome may be related to different neurodevelopment disorders. CASE PRESENTATION: We report a child with sexual developm...
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| Veröffentlicht in: | BMC Med Genomics |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8034074/ https://ncbi.nlm.nih.gov/pubmed/33832486 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-021-00934-x |
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