N. Gélvez

发表

The importance of fundus eye testing in rubella-induced deafness.

María Carolina Bermúdez Rey, S. Florez, M. Tamayo, 2013, International journal of pediatric otorhinolaryngology.

Risk factors associated with congenital defects that alter hearing or vision in children born in the city of Bogotá between 2002 and 2016.

F. Suárez-Obando, J. Ángel, P. Ayala-Ramírez, 2019, International journal of pediatric otorhinolaryngology.

Genetic association with intravitreal ranibizumab response for neovascular age-related macular degeneration in Hispanic population

Hernan A. Rios, F. Rodríguez, Shirley M Rosenstiehl, 2019, Taiwan journal of ophthalmology.

A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathy

F. Moreno, R. Santarelli, S. Berrettini, 2008, Human mutation.

Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: results of a screening program.

J. Frías, J. Bernal, S. Florez, 2009, International journal of pediatric otorhinolaryngology.

Allele-Specific Impairment of GJB2 Expression by GJB6 Deletion del(GJB6-D13S1854)

I. Schrijver, J. Rodriguez-Paris, M. Tamayo, 2011, PloS one.

Screening program for Waardenburg syndrome in Colombia: Clinical definition and phenotypic variability

M. Rodríguez, J. Bernal, S. Florez, 2008, American journal of medical genetics. Part A.

Mitochondrial DNA Studies Show Asymmetrical Amerindian Admixture in Afro-Colombian and Mestizo Populations

N. Gélvez, G. Keyeux, Clemencia Rodas, 2003, Human biology.

Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants.

Thomas L Casavant, Todd E Scheetz, E Ann Black-Ziegelbein, 2014, American journal of human genetics.

Detection of hearing loss in newborns: Definition of a screening strategy in Bogotá, Colombia.

María Carolina Bermúdez Rey, F. Suárez-Obando, G. López, 2019, International journal of pediatric otorhinolaryngology.

Molecular analyses of 2299delG and C759F mutations in Colombian Retinitis Pigmentosa and Sensorineural hearing loss affected individuals

G. López, S. Florez, M. Tamayo, 2014 .

Mutational analysis of the LDLR gene in a cohort of Colombian families with familial hypercholesterolemia.

A. I. Sánchez, Luz M Bernal, G. López, 2018, Atherosclerosis.

Transient evoked oto-acoustic emission screening in newborns in Bogotá, Colombia: a retrospective study.

Jorge Rojas, I. Zarante, J. Bernal, 2014, International journal of pediatric otorhinolaryngology.

Deafness on the island of Providencia - Colombia: different etiology, different genetic counseling.

M. Lattig, S. Plaza, J. Bernal, 2008, Genetic counseling.

Possible Migration Routes into South America Deduced from Mitochondrial DNA Studies in Colombian Amerindian Populations

D. Carter, N. Gélvez, G. Keyeux, 2002, Human biology.

Clinical and genetic characterization of RDH12-retinal dystrophy in a South American cohort.

G. Arno, M. Daich Varela, G. López, 2023, Ophthalmology. Retina.