Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|July 12, 2005
Unusual mixed gonadal dysgenesis associated with Müllerian duct persistence, polygonadia, and a 45,X/46,X,idic(Y)(p) karyotypeGloria Queipo, Karem Nieto, Patricia Grether, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|April 27, 2010
Detection of short-term chromosomal damage due to therapeutic 131I exposure in patients with thyroid cancerAngélica Hernández-Jardines, Bertha Molina, Victoria del Castillo, et al.
Journal of Toxicology and Environmental Health. Part A|June 4, 2015
NFE2L2 Gene Variants and Arsenic Susceptibility: A Lymphoblastoid ModelMirna E Morales-Marin, Emilio J Cordova, Federico Centeno, et al.
Cancer Genetics and Cytogenetics|October 11, 2005
Detection of ETV6 and RUNX1 gene rearrangements using fluorescence in situ hybridization in Mexican patients with acute lymphoblastic leukemia: experience at a single institutionPatricia Pérez-Vera, Oreth Montero-Ruiz, Sara Frías, et al.
American Journal of Respiratory and Critical Care Medicine|April 14, 2007
Local and circulating microchimerism is associated with hypersensitivity pneumonitisMartha L Bustos, Sara Frías, Sandra Ramos, et al.
Frontiers in Oncology|September 12, 2022
Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instabilityMoisés Ó Fiesco-Roa, Benilde García-de Teresa, Paula Leal-Anaya, et al.
Frontiers in Genetics|May 28, 2019
WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery PathwaysAlfredo Rodríguez, J Jesús Naveja, Leda Torres, et al.
Plos One|January 20, 2026
Prediction of myeloid malignant cells in Fanconi anemia using machine learningLuis A Flores-Mejía, Pablo Siliceo, Ulises Juárez Figueroa, et al.
Molecular Cytogenetics|November 28, 2017
7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotypeEmiy Yokoyama, Dennise Lesley Smith-Pellegrin, Silvia Sánchez, et al.
Theoretical Biology & Medical Modelling|September 20, 2015
Fanconi anemia cells with unrepaired DNA damage activate components of the checkpoint recovery processAlfredo Rodríguez, Leda Torres, Ulises Juárez, et al.
Pageof 3