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Biology|September 23, 2022
Prediction of Regulatory SNPs in Putative Minor Genes of the Neuro-Cardiovascular Variant in Fabry Reveals Insights into Autophagy/Apoptosis and FibrosisAndrea Virginia Ruiz Ramírez, Ernesto Prado Montes de Oca, Luis E FigueraBrain Sciences|March 29, 2023
Perceptions of Knowledge, Disease Impact and Predictive Genetic Testing in Family Members at Risk to Develop Early-Onset Alzheimer's Disease (EOAD) and Their Levels of Suicidal Ideation: A Mixed StudyYesica Arlae Reyes-Domínguez, Luis E Figuera, Aniel Jessica Leticia Brambila-TapiaClinical Genetics|February 1, 1993
Hyperkeratosis-hyperpigmentation syndrome: a confirmative caseL E Figuera, M A Rodríguez-Catellanos, A González-Mendoza, et al.Clinical Dysmorphology|October 29, 2002
Guadalajara camptodactyly type III: a new probably autosomal dominant syndromeL E Figuera, M L Ramírez-Dueñas, I P Dávalos, et al.Nature Genetics|June 1, 1995
Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1L E Figuera, M Pandolfo, P W Dunne, et al.American Journal of Medical Genetics|July 1, 1994
Spondyloepimetaphyseal dysplasia (SEMD) Shohat typeL E Figuera, M L Ramírez-Dueñas, M P Gallegos-Arreola, et al.American Journal of Medical Genetics|September 15, 1993
Schwartz-Jampel syndrome: an atypical form?L E Figuera, F J Jimenez-Gil, M O García-Cruz, et al.Annales De Genetique|January 1, 1996
Interstitial deletion 6q16.2q22.2 in a child with ectrodactylyL Correa-Cerro, D Garcíaz-Cruz, L Díaz-Castaños, et al.Clinical Genetics|January 1, 1993
Guadalajara camptodactyly syndrome type I. A corroborative familyL E Figuera, M L Ramírez-Dueñas, D García-Cruz, et al.Clinical Dysmorphology|June 9, 2006
Interstitial deletion of 13q22-->q31: case report and review of the literatureJosé A Morales, Adriana P Mendizabal, Ana I Vásquez, et al.Pageof 12