Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
European Archives of Paediatric Dentistry : Official Journal of the European Academy of Paediatric Dentistry|November 30, 2011
Case report: identical twins revealing discordant hypodontia. The rationale of dental arch differences in monozygotic twinsM Varela, M J Trujillo-Tiebas, P Garcia-Camba
Journal of Neurogenetics|March 26, 2008
Two non-contiguous duplications in the DMD gene in a Spanish familyM Fenollar-Cortés, J Gallego-Merlo, M J Trujillo-Tiebas, et al.
Actas Dermo-Sifiliograficas|November 29, 2017
Genetic diagnosis of epidermolysis bullosa: recommendations from an expert Spanish research groupC Sánchez-Jimeno, M J Escámez, C Ayuso, et al.
Journal of Assisted Reproduction and Genetics|May 26, 2006
Prenatal diagnosis of 46, XX male fetusM J Trujillo-Tiebas, C González-González, I Lorda-Sánchez, et al.
Archivos De La Sociedad Espanola De Oftalmologia|April 20, 2013
Guidelines for genetic study of aniridiaF Blanco-Kelly, C Villaverde-Montero, I Lorda-Sánchez, et al.
Journal of Assisted Reproduction and Genetics|October 1, 2009
Prenatal diagnosis of skeletal dysplasia due to FGFR3 gene mutations: a 9-year experience : prenatal diagnosis in FGFR3 geneM J Trujillo-Tiebas, M Fenollar-Cortés, I Lorda-Sánchez, et al.
Molecular Genetics and Metabolism Reports|November 23, 2016
Nine-year experience in Gaucher disease diagnosis at the Spanish reference center Fundación Jiménez DíazN V Ortiz-Cabrera, J Gallego-Merlo, C Vélez-Monsalve, et al.
European Journal of Neurology|December 4, 2008
Prenatal diagnosis of Huntington disease in maternal plasma: direct and indirect studyA Bustamante-Aragones, M J Trujillo-Tiebas, J Gallego-Merlo, et al.
Molecular Vision|February 6, 2007
Partial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt diseaseR Riveiro-Alvarez, D Valverde, I Lorda-Sanchez, et al.
Pageof 2