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

Crossref DOI link: https://doi.org/10.1038/gim.2017.162

Published Print: 2018-06

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

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
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Text and Data Mining valid from 2018-06-01

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This article is maintained by: Elsevier

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

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2017.162

Content Type: article

Copyright: © 2018, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics

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