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Craniofacial features of 3q29 deletion syndrome: Application of next‐generation phenotyping technology
3q29 deletion syndrome (3q29del) is a recurrent deletion syndrome associated with neuropsychiatric disorders and congenital anomalies. Dysmorphic facial features have been described but not systematically characterized. This study aims to detail the 3q29del craniofacial phenotype and use a machine l...
Tallennettuna:
| Julkaisussa: | Am J Med Genet A |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
John Wiley & Sons, Inc.
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8250870/ https://ncbi.nlm.nih.gov/pubmed/33938623 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.62227 |
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