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Whole genome paired-end sequencing elucidates functional an..:
Schluth-Bolard, Caroline, Schluth
;
Diguet, Flavie
;
Chatron, Nicolas
...
info:eu-repo/semantics/altIdentifier/doi/10.1136/jmedgenet-2018-105778. , 2019
Link:
https://hal.science/hal-03863519
RT Journal T1
Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders
UL https://suche.suub.uni-bremen.de/peid=base-ftnormandieuniv:oai:HAL:hal-03863519v1&Exemplar=1&LAN=DE A1 Schluth-Bolard, Caroline, Schluth A1 Diguet, Flavie A1 Chatron, Nicolas A1 Rollat-Farnier, Pierre-Antoine A1 Bardel, Claire A1 Afenjar, Alexandra A1 Amblard, Florence A1 Amiel, Jeanne A1 Blesson, Sophie A1 Callier, Patrick A1 Capri, Yline A1 Collignon, Patrick A1 Cordier, Marie-Pierre A1 Coubes, Christine A1 Demeer, Bénédicte A1 Chaussenot, Annabelle A1 Demurger, Florence A1 Devillard, Françoise A1 Doco-Fenzy, Martine A1 Dupont, Celine A1 Dupont, Jean-Michel A1 Dupuis-Girod, Sophie A1 Faivre, Laurence A1 Gilbert-Dussardier, Brigitte A1 Guerrot, Anne-Marie A1 Houlier, Marine A1 Isidor, Bertrand A1 Jaillard, Sylvie A1 Joly-Helas, Géraldine A1 Kremer, Valérie A1 Lacombe, Didier A1 Le Caignec, Cedric A1 Lebbar, Aziza A1 Lebrun, Marine A1 Lesca, Gaetan A1 Lespinasse, James A1 Levy, Jonathan A1 Malan, Valérie A1 Mathieu-Dramard, Michèle A1 Masson, Julie A1 Masurel-Paulet, Alice A1 Mignot, Cyril A1 Missirian, Chantal A1 Morice-Picard, Fanny A1 Moutton, Sébastien A1 Nadeau, Gwenaël A1 Pebrel-Richard, Céline A1 Odent, Sylvie A1 Paquis-Flucklinger, Véronique A1 Pasquier, Laurent A1 Philip, Nicole A1 Plutino, Morgane A1 Pons, Linda A1 Portnoi, Marie-France A1 Prieur, Fabienne A1 Puechberty, Jacques A1 Putoux, Audrey A1 Rio, Marlène A1 Rooryck-Thambo, Caroline A1 Rossi, Massimiliano A1 Sarret, Catherine A1 Satre, Veronique A1 Siffroi, Jean-Pierre A1 Till, Marianne A1 Touraine, Renaud A1 Toutain, Annick A1 Toutain, Jérôme A1 Valence, Stephanie A1 Verloes, Alain A1 Whalen, Sandra A1 Edery, Patrick A1 Tabet, Anne-Claude A1 Sanlaville, Damien PB HAL CCSD; BMJ Publishing Group YR 2019 K1 intellectual disability K1 chromosomal rearrangements K1 whole genome sequencing K1 structural variation K1 position effect K1 [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics JF info:eu-repo/semantics/altIdentifier/doi/10.1136/jmedgenet-2018-105778 LK http://dx.doi.org/https://hal.science/hal-03863519 DO https://hal.science/hal-03863519 SF ELIB - SuUB Bremen
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