Martine Doco Fenzy
AuthID: R-00G-MPJ
1
TÃTULO: CDK13-related disorder: Report of a series of 18 previously unpublished individuals and description of an epigenetic signature
AUTORES: Rouxel, Flavien; Relator, Raissa; Kerkhof, Jennifer; McConkey, Haley; Levy, Michael; Dias, Patricia; Barat Houari, Mouna; Bednarek, Nathalie; Boute, Odile; Chatron, Nicolas; Cherik, Florian; Delahaye Duriez, Andree; Doco Fenzy, Martine; Faivre, Laurence; Gauthier, Lucas W.; Heron, Delphine; Hildebrand, Michael S.; Lesca, Gaetan; Lespinasse, James; Mazel, Benoit; ...Mais
PUBLICAÇÃO: 2022, FONTE: GENETICS IN MEDICINE, VOLUME: 24, NÚMERO: 5
AUTORES: Rouxel, Flavien; Relator, Raissa; Kerkhof, Jennifer; McConkey, Haley; Levy, Michael; Dias, Patricia; Barat Houari, Mouna; Bednarek, Nathalie; Boute, Odile; Chatron, Nicolas; Cherik, Florian; Delahaye Duriez, Andree; Doco Fenzy, Martine; Faivre, Laurence; Gauthier, Lucas W.; Heron, Delphine; Hildebrand, Michael S.; Lesca, Gaetan; Lespinasse, James; Mazel, Benoit; ...Mais
PUBLICAÇÃO: 2022, FONTE: GENETICS IN MEDICINE, VOLUME: 24, NÚMERO: 5
INDEXADO EM: 
Scopus 
WOS
Scopus WOS2
TÃTULO: Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth
AUTORES: Lionel Van Maldergem; Qingming M Hou; Vera M Kalscheuer; Marlene Rio; Martine Doco Fenzy; Ana Medeira; Arjan P M de Brouwer; Christelle Cabrol; Stefan A Haas; Pierre Cacciagli; Sebastien Moutton; Emilie Landais; Jacques Motte; Laurence Colleaux; Celine Bonnet; Laurent Villard; Juliette Dupont; Heng Ye Man;
PUBLICAÇÃO: 2013, FONTE: HUMAN MOLECULAR GENETICS, VOLUME: 22, NÚMERO: 16
AUTORES: Lionel Van Maldergem; Qingming M Hou; Vera M Kalscheuer; Marlene Rio; Martine Doco Fenzy; Ana Medeira; Arjan P M de Brouwer; Christelle Cabrol; Stefan A Haas; Pierre Cacciagli; Sebastien Moutton; Emilie Landais; Jacques Motte; Laurence Colleaux; Celine Bonnet; Laurent Villard; Juliette Dupont; Heng Ye Man;
PUBLICAÇÃO: 2013, FONTE: HUMAN MOLECULAR GENETICS, VOLUME: 22, NÚMERO: 16
