Browsing by Author Andrieux, Joris

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 3 of 3
Issue DateTitleAuthor(s)Citation
20167p22.1 microdeletions involving ACTB associated with developmental delay, short stature, and microcephalyBrescianini, Sally; Andrieux, Joris; De Paepe, Anne; Doumoto, Tomotsune; Edwards, Matthew; Narai, Satoshi; Petit, Florence; Sangu, Noriko; Shimojima, Keiko; Togawa, Masami; Vanakker, Olivier; Whitehall, John; Yamamoto, Toshiyuki; Not known7p22.1 microdeletions involving ACTB associated with developmental delay, short stature, and microcephaly, European Journal of Medical Genetics; formerly Annales de Genetique (France) (0003-3995), vol.59, 10, 2016,pp 502-506
20167p22.1 microdeletions involving ACTB associated with developmental delay, short stature, and microcephalyBrescianini, Sally; Andrieux, Joris; De Paepe, Anne; Doumoto, Tomotsune; Edwards, Matthew; Narai, Satoshi; Petit, Florence; Sangu, Noriko; Shimojima, Keiko; Togawa, Masami; Vanakker, Olivier; Whitehall, John; Yamamoto, Toshiyuki; Not known7p22.1 microdeletions involving ACTB associated with developmental delay, short stature, and microcephaly, European Journal of Medical Genetics; formerly Annales de Genetique (France) (0003-3995), vol.59, 10, 2016,pp 502-506
2015Clinical and Molecular Characterization of the 20q11.2 Microdeletion Syndrome: Six New PatientsEwans, Lisa; Wilson, Meredith; Andrieux, Joris; Crolla, John; Demeer, Benedicte; et al, Various; Foulds, Nicola; Jedraszak, Guillaume; Mathieu-Dramard, Michele; Maye, Una; Receveur, Aline; Temple, Ik; Weber, Astrid; Children's Hospital Westmead: Genetic Medicine; Childrens Hospital Westmead: Paediatrics & Child HealthClinical and Molecular Characterization of the 20q11.2 Microdeletion Syndrome: Six New Patients, American Journal of Medical Genetics. Part A, vol.167A, 3, 2015,pp 504-511