Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis-Reference-Cited by-同舟云学术

Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis

Published:2018-06 Issue:6 Volume:20 Page:645-654
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Nambot Sophie,Thevenon Julien,Kuentz Paul,Duffourd Yannis,Tisserant Emilie,Bruel Ange-Line,Mosca-Boidron Anne-Laure,Masurel-Paulet Alice,Lehalle Daphné,Jean-Marçais Nolwenn,Lefebvre Mathilde,Vabres Pierre,El Chehadeh-Djebbar Salima,Philippe Christophe,Tran Mau-Them Frederic,St-Onge Judith,Jouan Thibaud,Chevarin Martin,Poé Charlotte,Carmignac Virginie,Vitobello Antonio,Callier Patrick,Rivière Jean-Baptiste,Faivre Laurence,Thauvin-Robinet Christel

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim2017162.pdf

Reference42 articles.

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