Search research articles
Contact Us
Filters
Showing results (1-10 of 86) with videos related to
Page
of 9
Sort By:
Community Genetics
|
November 13, 2004
Genetic services in Mexico City
Susana Kofman-Alfaro, Juan Carlos Zenteno
Molecular Vision
|
April 18, 2006
PAX6 gene intragenic deletions in Mexican patients with congenital aniridia
Arturo Ramirez-Miranda, Juan Carlos Zenteno
Gaceta Medica De Mexico
|
May 6, 2017
[Gene therapy for vision restoration in patients with Leber congenital amaurosis (LCA) due to RPE65 gene mutations: beginning the phase IV trial]
Óscar Francisco Chacón-Camacho, Juan Carlos Zenteno
World Journal of Clinical Cases
|
February 17, 2015
Review and update on the molecular basis of Leber congenital amaurosis
Oscar Francisco Chacon-Camacho, Juan Carlos Zenteno
Ophthalmic Genetics
|
December 29, 2007
A new GJA1 (connexin 43) mutation causing oculodentodigital dysplasia associated to uncommon features
David Rivera de la Parra, Juan Carlos Zenteno
Molecular Vision
|
September 26, 2007
The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy
Vicente Correa-Gomez, Leonardo Villalvazo-Cordero, Juan Carlos Zenteno
Molecular Vision
|
September 27, 2013
The T allele of lysyl oxidase-like 1 rs41435250 is a novel risk factor for pseudoexfoliation syndrome and pseudoexfoliation glaucoma independently and through intragenic epistatic interaction
Dalia Guadarrama-Vallejo, Antonio Miranda-Duarte, Juan Carlos Zenteno
American Journal of Medical Genetics. Part A
|
August 8, 2006
Anophthalmia-esophageal atresia syndrome caused by an SOX2 gene deletion in monozygotic twin brothers with markedly discordant phenotypes
Juan Carlos Zenteno, Hector J Perez-Cano, Monica Aguinaga
Archives of Gynecology and Obstetrics
|
June 29, 2004
Molecular analysis of the anti-Müllerian hormone, the anti-Müllerian hormone receptor, and galactose-1-phosphate uridyl transferase genes in patients with the Mayer-Rokitansky-Küster-Hauser syndrome
Juan Carlos Zenteno, Sebastian Carranza-Lira, Susana Kofman-Alfaro
Gaceta Medica De Mexico
|
August 21, 2015
[Gene therapy for hereditary ophthalmological diseases: Advances and future perspectives]
Óscar Francisco Chacón-Camacho, Aline Astorga-Carballo, Juan Carlos Zenteno
Page
of 9
Search research articles
Search
Showing results (1-10 of 86) with videos related to
Sort By:
Page
of 9
Community Genetics
|
November 13, 2004
Genetic services in Mexico City
Susana Kofman-Alfaro, Juan Carlos Zenteno
Molecular Vision
|
April 18, 2006
PAX6 gene intragenic deletions in Mexican patients with congenital aniridia
Arturo Ramirez-Miranda, Juan Carlos Zenteno
Gaceta Medica De Mexico
|
May 6, 2017
[Gene therapy for vision restoration in patients with Leber congenital amaurosis (LCA) due to RPE65 gene mutations: beginning the phase IV trial]
Óscar Francisco Chacón-Camacho, Juan Carlos Zenteno
World Journal of Clinical Cases
|
February 17, 2015
Review and update on the molecular basis of Leber congenital amaurosis
Oscar Francisco Chacon-Camacho, Juan Carlos Zenteno
Ophthalmic Genetics
|
December 29, 2007
A new GJA1 (connexin 43) mutation causing oculodentodigital dysplasia associated to uncommon features
David Rivera de la Parra, Juan Carlos Zenteno
Molecular Vision
|
September 26, 2007
The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy
Vicente Correa-Gomez, Leonardo Villalvazo-Cordero, Juan Carlos Zenteno
Molecular Vision
|
September 27, 2013
The T allele of lysyl oxidase-like 1 rs41435250 is a novel risk factor for pseudoexfoliation syndrome and pseudoexfoliation glaucoma independently and through intragenic epistatic interaction
Dalia Guadarrama-Vallejo, Antonio Miranda-Duarte, Juan Carlos Zenteno
American Journal of Medical Genetics. Part A
|
August 8, 2006
Anophthalmia-esophageal atresia syndrome caused by an SOX2 gene deletion in monozygotic twin brothers with markedly discordant phenotypes
Juan Carlos Zenteno, Hector J Perez-Cano, Monica Aguinaga
Archives of Gynecology and Obstetrics
|
June 29, 2004
Molecular analysis of the anti-Müllerian hormone, the anti-Müllerian hormone receptor, and galactose-1-phosphate uridyl transferase genes in patients with the Mayer-Rokitansky-Küster-Hauser syndrome
Juan Carlos Zenteno, Sebastian Carranza-Lira, Susana Kofman-Alfaro
Gaceta Medica De Mexico
|
August 21, 2015
[Gene therapy for hereditary ophthalmological diseases: Advances and future perspectives]
Óscar Francisco Chacón-Camacho, Aline Astorga-Carballo, Juan Carlos Zenteno
Page
of 9