Clinical and molecular characterization of 12 prenatal cases of Cri‐du‐chat syndrome

BACKGROUND: This study aimed to define the molecular basis for 12 prenatal cases of Cri‐du‐chat syndrome (CdCS) and the potential genotyping‐phenotyping association. METHODS: Karyotyping and single nucleotide polymorphism array analyses for copy number variants were performed. RESULTS: Nine cases ha...

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Detalles Bibliográficos
Autores principales: Peng, Ying, Pang, Jialun, Hu, Jiancheng, Jia, Zhengjun, Xi, Hui, Ma, Na, Yang, Shuting, Liu, Jing, Huang, Xiaoliang, Tang, Chengyuan, Wang, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434726/
https://www.ncbi.nlm.nih.gov/pubmed/32500674
http://dx.doi.org/10.1002/mgg3.1312

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434726/
https://www.ncbi.nlm.nih.gov/pubmed/32500674
http://dx.doi.org/10.1002/mgg3.1312

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