首页> The Journal of international medical research> Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of 18q12.3 encompassing SETBP1.

Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of 18q12.3 encompassing SETBP1.

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第一作者： Yaqing,Zhou

第一单位： Reproductive Center Laboratory, Ninghai County Maternal and Child Health Hospital, Ningbo, Zhejiang, PR China.

作者： Yaqing,Zhou ^[1] ; Yan,Quan ^[2] ; Yijun,Wu ^[3] ; Yinxing,Zhang ^[4]

作者单位： Reproductive Center Laboratory, Ninghai County Maternal and Child Health Hospital, Ningbo, Zhejiang, PR China. ^[1] Department of Maternal Health Care, Shiyan Maternal and Child Health Hospital, Shiyan, Hubei, PR China. ^[2] Department of Obstetrics, Huanggang Central Hospital, Huanggang, Hubei, PR China. ^[3] Department of Obstetrics and Gynecology, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Edong Healthcare Group, Huangshi, Hubei, PR China. ^[4]

关键词 Chromosomal microarray analysis SET binding protein 1 autosomal dominant 29 chromosomal microdeletion chromosomal microduplication intellectual developmental disorder prenatal diagnosis