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Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review.

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作者单位: Cochin Institute, INSERM U1016, Paris, France. [1] Cytogenetics Department, APHP, Cochin Hospital, Paris Descartes University, Paris, France. [2] Cytogenetics and Cell Biology Department, Rennes University Hospital, Rennes, France. [3] Medical Genetics Department, Lille Hospital, Lille, France. [4] Medical Genetics Department, Rennes University Hospital, Rennes, France. [5] Department of Genetics, APHP-Robert Debré University Hospital, Paris, France. [6] Pediatrician, Oran, Algeria. [7] Department of Genetics, Tours University Hospital, Tours, France. [8] Department of Pathology, CHU Brest, France. [9] Department of Genetics, Arras Hospital, Arras, France. [10] Department of Medical Genetics, CHBA, Vannes, France. [11] Department of Pediatrics, Saint-Brieuc Hospital, Saint-Brieuc, France. [12] Department of Anatomy and Cell Pathology, CHRU Lille, France. [13] Molecular Genetics Department, Rennes University Hospital, Rennes, France. [14] UMR 6290, IGDR, Medical School, Rennes, France. [15] Department of Genetics, APHP, Necker-Enfants Malades University Hospital, Paris, France. [16] Laboratory of Cytogenetics, APHP, Necker-Enfants Malades Hospital, Paris Descartes University, Paris, France. [17] Department of Pediatrics, Jean-Verdier Hospital, APHP, Paris 13 University, Bondy, France. [18] Department of Genetics, Raymond Poincaré University Hospital, Garches, France. [19] Department of Neuropediatrics, Raymond Poincaré University Hospital, Garches, France. [20] Cytogenetics, APHP, Jean-Verdier University Hospital, Bondy; Paris 13, Sorbonne Paris Cité, UFR SMBH, Bobigny, France; Inserm, U676, Paris, France. [21] INSERM U676, and Paris VII-Denis Diderot Medical School, Paris, France. [22]
DOI 10.1002/ajmg.a.36932
PMID 25847481
发布时间 2020-09-30
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American journal of medical genetics. Part A

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