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Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndrome.

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第一作者: Hiromi,Aoi
第一单位: Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.;Department of Obstetrics and Gynecology, Juntendo University, Tokyo, Japan.
作者单位: Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.;Department of Obstetrics and Gynecology, Juntendo University, Tokyo, Japan. [1] Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan. [2] Clinical Genetics Unit, Instituto da Crianca, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Brazil. [3] Department of Pediatrics, University Hospital, Faculty of Medicine, Kagawa University, Kagawa, Japan. [4] Department of Obstetrics and Gynecology, Juntendo University, Tokyo, Japan. [5] Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.;Department of Oncology, Yokohama City University Graduate School of Medicine, Yokohama, Japan. [6] Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.;Clinical Genetics Department, Yokohama City University Hospital, Yokohama, Japan. [7] Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan. naomat@yokohama-cu.ac.jp. [8]
DOI 10.1038/s10038-019-0643-z
PMID 31337854
发布时间 2025-01-03
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Journal of human genetics

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