C. Gil-Rodrı́guez's Profile

Role	Title	Level	Year	L/R
🐜	Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation. 18 auth. M. Deardorff, M. Kaur, Dinah Yaeger, Abhinav Rampuria, S. Korolev, J. Pié, C. Gil-Rodrı́guez, María Arnedo, B. Loeys, A. Kline, ... Meredith Wilson, K. Lillquist, V. Siu, F. Ramos, A. Musio, L. Jackson, D. Dorsett, I. Krantz	9	2007	9 🐜
🐬	The possible origin of Zostera noltii in the Canary Islands and guidelines for restoration O. Diekmann, Licínia Gouveia, J. Pérez, C. Gil-Rodrı́guez, E. Serrão	4	2010	4 🐬
🐜	Truncating mutations in THAP1 define the nuclear localization signal 15 auth. Alma Osmanovic, A. Dendorfer, Alev Erogullari, Nils Uflacker, D. Braunholz, A. Rakovic, G. Vierke, C. Gil-Rodrı́guez, A. Münchau, M. Albrecht, ... N. Brüggemann, G. Gillessen‐Kaesbach, C. Klein, K. Lohmann, F. Kaiser	3	2011	3 🐜
🦁	De Novo Heterozygous Mutations in SMC 3 Cause a Range of Cornelia de Lange Syndrome-Overlapping Phenotypes Marı́a 62 auth. C. Gil-Rodrı́guez, M. Deardorff, Morad Ansari, C. Tan, I. Parenti, C. Baquero‐Montoya, L. Ousager, B. Puisac, M. Hernández-Marcos, Esperanza Teresa-Rodrigo, Í. Marcos-Alcalde, J. Wesselink, Silvia Lusa-Bernal, E. Bijlsma, D. Braunholz, ... I. Bueno-Martínez, Dinah Clark, N. Cooper, C. Curry, R. Fisher, A. Fryer, J. Ganesh, C. Gervasini, G. Gillessen‐Kaesbach, Yiran Guo, H. Hakonarson, R. Hopkin, M. Kaur, B. Keating, M. Kibaek, E. Kinning, T. Kleefstra, A. Kline, E. Kuchinskaya, L. Larizza, Yun R Li, Xuanzhu Liu, M. Mariani, J. Picker, Á. Pié, J. Pozojevic, E. Queralt, J. Richer, E. Roeder, Anubha Sinha, R. Scott, J. So, Katie Wusik, L. Wilson, Jianguo Zhang, P. Gómez-Puertas, C. Casale, L. Ström, A. Selicorni, F. Ramos, L. Jackson, I. Krantz, Soma Das, R. Hennekam, F. Kaiser, D. FitzPatrick, J. Pié	0	2015	0 🦁