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OMIXCARE: OMICS technologies solved about 33% of the patien..:
Colin, Estelle
;
Duffourd, Yannis
;
Tisserant, Emilie
...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fcell.2022.1021785. , 2022
Link:
https://univ-rennes.hal.science/hal-03886419
RT Journal T1
OMIXCARE: OMICS technologies solved about 33% of the patients with heterogeneous rare neuro-developmental disorders and negative exome sequencing results and identified 13% additional candidate variants
UL https://suche.suub.uni-bremen.de/peid=base-ftanrparis:oai:HAL:hal-03886419v1&Exemplar=1&LAN=DE A1 Colin, Estelle A1 Duffourd, Yannis A1 Tisserant, Emilie A1 Relator, Raissa A1 Bruel, Ange-Line A1 Tran Mau-Them, Frédéric A1 Denommé-Pichon, Anne-Sophie A1 Safraou, Hana A1 Delanne, Julian A1 Jean-Marçais, Nolwenn A1 Keren, Boris A1 Isidor, Bertrand A1 Vincent, Marie A1 Mignot, Cyril A1 Heron, Delphine A1 Afenjar, Alexandra A1 Heide, Solveig A1 Faudet, Anne A1 Charles, Perrine A1 Odent, Sylvie A1 Herenger, Yvan A1 Sorlin, Arthur A1 Moutton, Sébastien A1 Kerkhof, Jennifer A1 Mcconkey, Haley A1 Chevarin, Martin A1 Poë, Charlotte A1 Couturier, Victor A1 Bourgeois, Valentin A1 Callier, Patrick A1 Boland, Anne A1 Olaso, Robert A1 Philippe, Christophe A1 Sadikovic, Bekim A1 Thauvin-Robinet, Christel A1 Faivre, Laurence A1 Deleuze, Jean-François A1 Vitobello, Antonio PB HAL CCSD; Frontiers media YR 2022 K1 DNA methylation analysis K1 genome sequencing K1 transcriptome sequencing K1 translational research K1 undiagnosed neurodevelopmental diseases K1 [SDV.GEN]Life Sciences [q-bio]/Genetics JF info:eu-repo/semantics/altIdentifier/doi/10.3389/fcell.2022.1021785 LK http://dx.doi.org/https://univ-rennes.hal.science/hal-03886419 DO https://univ-rennes.hal.science/hal-03886419 SF ELIB - SuUB Bremen
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