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...

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Bibliografiske detaljer
Udgivet i:Am J Med Genet A
Main Authors: Mak, Bryan C., Sanchez Russo, Rossana, Gambello, Michael J., Fleischer, Nicole, Black, Emily D., Leslie, Elizabeth, Murphy, Melissa M., Mulle, Jennifer Gladys
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley & Sons, Inc. 2021
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Original Articles
Online adgang: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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