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Cerebral White Matter Lesions and Dysmorphisms: Signs Suggestive of 6p25 Deletion Syndrome—Literature Review
Deletion of the region including chromosome 6p25 has been defined as a syndrome, with more than 68 reported cases. Individuals affected by the syndrome exhibit variable findings, including developmental delay and intellectual disability, cardiac anomalies, dysmorphic features, and—less commonly—skel...
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| Vydáno v: | J Pediatr Genet |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Georg Thieme Verlag KG
2019
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6824910/ https://ncbi.nlm.nih.gov/pubmed/31687258 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0039-1694015 |
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