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CNS Spectrums|November 8, 2005
An 8q21 deletion in a patient with comorbid psychosis and mental retardationNora Urraca, Maria de la Luz Arenas-Sordo, Abigail Ortiz-Dominguez, et al.
Gaceta Medica De Mexico|February 6, 2008
[Strategies for clinical and molecular diagnosis of Charcot-Marie-Tooth 1A among Mexican patients]Edgar Hernández-Zamora, Maria de la Luz Arenas-Sordo, Rosa Elena Escobar-Cedillo, et al.
European Journal of Radiology|November 25, 2025
Temporal bone and multisystem phenotypic stratification in oculo-auriculo-vertebral spectrum using high-resolution CT: Correlation with tasse severity scoreMaria-de-la-Luz Arenas-Sordo, Garly-Daniel Gonzalez-Rosado, Maria-Isabel Barradas-Hernandez, et al.
International Journal of Pediatric Otorhinolaryngology|August 29, 2012
Unique spectrum of GJB2 mutations in MexicoMaria de la Luz Arenas-Sordo, Ibis Menendez, Edgar Hernández-Zamora, et al.
International Journal of Pediatric Otorhinolaryngology|October 2, 2017
Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohortFiliz Basak Cengiz, Rasim Yilmazer, Levent Olgun, et al.
Human Genetics|June 20, 2021
Unraveling the genetic complexities of combined retinal dystrophy and hearing impairmentPaulina Bahena, Narsis Daftarian, Reza Maroofian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2015
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohortGuney Bademci, Joseph Foster, Nejat Mahdieh, et al.
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