Items where Author is "Brachet, Cécile"
Number of items: 2. 2016Coppieters, Frauke and Ascari, Giulia and Dannhausen, Katharina and Nikopoulos, Konstantinos and Peelman, Frank and Karlstetter, Marcus and Xu, Mingchu and Brachet, Cécile and Meunier, Isabelle and Tsilimbaris, Miltiadis K. and Tsika, Chrysanthi and Blazaki, Styliani V. and Vergult, Sarah and Farinelli, Pietro and Van Laethem, Thalia and Bauwens, Miriam and De Bruyne, Marieke and Chen, Rui and Langmann, Thomas and Sui, Ruifang and Meire, Françoise and Rivolta, Carlo and Hamel, Christian P. and Leroy, Bart P. and De Baere, Elfride. (2016) Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination. American Journal of Human Genetics, 99 (2). pp. 470-480. 2011Brachet, Cécile and Birk, Julia and Christophe, Catherine and Tenoutasse, Sylvie and Velkeniers, Brigitte and Heinrichs, Claudine and Rutishauser, Jonas. (2011) Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene. European journal of endocrinology, Vol. 164, H. 2. pp. 179-187. |
