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

Abstract 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 ca...

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Dades bibliogràfiques

Autors principals:	Ying Peng, Jialun Pang, Jiancheng Hu, Zhengjun Jia, Hui Xi, Na Ma, Shuting Yang, Jing Liu, Xiaoliang Huang, Chengyuan Tang, Hua Wang
Format:	Artigo
Idioma:	Inglês
Publicat:	Wiley 2020-08-01
Col·lecció:	Molecular Genetics & Genomic Medicine
Matèries:	5p deletion Cri‐du‐chat syndrome prenatal diagnosis single nucleotide polymorphism array
Accés en línia:	https://doi.org/10.1002/mgg3.1312
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