作者单位：
Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR1163, Imagine Institute, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Pediatric Neurology APHP- Necker Enfants Malades University Hospital, Paris, France.
[1]
Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR1163, Imagine Institute, Paris, France.
[2]
Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR1163, Imagine Institute, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.
[3]
Department of Obstetrics and Fetal Medicine APHP- Necker Enfants Malades University Hospital, Paris, France.
[4]
Genomic Core Facility, INSERM UMR1163, Imagine Institute, Paris, France.
[5]
Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Laboratory of Inherited Kidney Diseases, INSERM UMR1163, Imagine Institute, Paris, France; Paris Diderot University, 75013, Paris, France.
[6]
Bioinformatic Core Facility, INSERM UMR1163, Imagine Institute, Paris, France.
[7]
Pediatric Radiology, APHP-Necker Enfants Malades University Hospital, Paris, France; Image- Institut Imagine, INSERM UMR1163, Université Paris Descartes, Hôpital Necker Enfants Malades, Paris, France.
[8]
Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR1163, Imagine Institute, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Pediatric Neurology APHP- Necker Enfants Malades University Hospital, Paris, France; Centre de Référence, Déficiences Intellectuelles de Causes Rares, APHP- Necker Enfants Malades University Hospital, Paris, France. Electronic address: nadia.bahi-buisson@nck.aphp.fr.
[9]
DOI
10.1016/j.ejmg.2018.08.001
PMID
30121372
发布时间
2021-02-26
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