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Molecular Vision|September 1, 2010
Different phenotypes of lattice corneal dystrophy type I in patients with 417C>T (R124C) and 1762A>G (H572R) mutations in TGFBI (BIGH3)Pablo Romero, Mauricio Moraga, Luisa HerreraRevista Chilena De Pediatria|March 14, 2017
[Clinical and genetic study patients with tuberous sclerosis complex]Carla Rubilar, Francisca López, Mónica Troncoso, et al.Molecular Vision|August 19, 2011
c.194 A>C (Q65P) mutation in the LMX1B gene in patients with nail-patella syndrome associated with glaucomaPablo Romero, Felipe Sanhueza, Pamela Lopez, et al.Molecular Biology Reports|October 30, 2020
Morphotype divergence and genetic diversity of Hedeoma piperita Benth. in western MexicoMaría Luisa Herrera-Arroyo, Yessica Rico, Brenda Y Bedolla-GarcíaRevista Medica De Chile|November 29, 2017
[Abnormal expansion of C9orf72 gene in familial frontotemporal dementia]Marcelo Miranda C, M Leonor Bustamante C, Luisa Herrera CFrontiers in Human Neuroscience|September 29, 2022
Potential epigenetic mechanisms in psychotherapy: a pilot study on DNA methylation and mentalization change in borderline personality disorderYamil Quevedo, Linda Booij, Luisa Herrera, et al.Molecular Vision|May 13, 2008
Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) genePablo Romero, Marlene Vogel, Jose-Manuel Diaz, et al.Acta Psychologica|June 26, 2026
Cognitive reappraisal is associated with reduced threat expectancy during social fear extinctionViviana Miño, Felix Bacigalupo, Vanetza E Quezada-Scholz, et al.Clinical Case Reports|May 24, 2021
Hypomyelination and Congenital Cataract: Identification of a Novel likely pathogenic c.414+1G>A in FAM126A gene VariantMónica Troncoso, Fernanda Balut, Scarlet Witting, et al.American Journal of Medical Genetics|September 5, 2002
Genes and translocations involved in POFDavid Schlessinger, Luisa Herrera, Laura Crisponi, et al.Pageof 4