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Marisa Cruz

Showing results (31-40 of 35) with videos related to

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Journal of Human Genetics|September 6, 2018
Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencingDiana Matías-Pérez, Leopoldo A García-Montaño, Marisa Cruz-Aguilar, et al.
Molecular Genetics & Genomic Medicine|November 19, 2019
Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next-generation sequencingJuan C Zenteno, Leopoldo A García-Montaño, Marisa Cruz-Aguilar, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|May 16, 2024
Do Acoustic Characteristics of Dysarthria in People With Parkinson's Disease Differ Across Languages?Serge Pinto, Rita Cardoso, Cyril Atkinson-Clement, et al.
Human Molecular Genetics|April 16, 2019
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndromeDaniel Berner, Ursula Hoja, Matthias Zenkel, et al.
Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Journal of Human Genetics|September 6, 2018
Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencingDiana Matías-Pérez, Leopoldo A García-Montaño, Marisa Cruz-Aguilar, et al.
Molecular Genetics & Genomic Medicine|November 19, 2019
Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next-generation sequencingJuan C Zenteno, Leopoldo A García-Montaño, Marisa Cruz-Aguilar, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|May 16, 2024
Do Acoustic Characteristics of Dysarthria in People With Parkinson's Disease Differ Across Languages?Serge Pinto, Rita Cardoso, Cyril Atkinson-Clement, et al.
Human Molecular Genetics|April 16, 2019
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndromeDaniel Berner, Ursula Hoja, Matthias Zenkel, et al.
Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.
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