Prenatal diagnosis and genetic counseling of an inherited Xq24q25 deletion associated with normal phenotype

Zhou, YQ; Zhang, MX; Zhu, YM; Zhao, Q

Zhao, Q (通讯作者)，Dongsheng Area Peoples Hosp, Dept Clin Lab, Ordos, Inner Mongolia, Peoples R China.

MOLECULAR CYTOGENETICS, 2022; 15 (1):

Abstract

Background Copy number variants (CNVs) are an important source of normal and pathogenic genome variations. CNVs identified in prenatal cases need care......

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