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Publications by David Velásquez

Noncoding Mutations of HGF Are Associated With Nonsyndromic Hearing Loss, DFNB39

American Journal of Human Genetics

English

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Molecular Analysis of Mitochondrial Gene Mutations in Korean Patients With Nonsyndromic Hearing Loss

International Journal of Molecular Medicine

English

Recessive Mutations of TMC1 Associated With Moderate to Severe Hearing Loss

Molecular Neuroscience

English

Screening of Connexin 26 in Nonsyndromic Hearing Loss

International Archives of Otorhinolaryngology

Otorhinolaryngology

English

Presymptomatic Diagnosis of Nonsyndromic Hearing Loss by Genotyping

Archives of Otolaryngology–Head & Neck Surgery

English

Mutations of P4HA2 Encoding Prolyl 4-Hydroxylase 2 Are Associated With Nonsyndromic High Myopia

Genetics in Medicine

English

Histopathology of Nonsyndromic Autosomal Dominant Midfrequency Sensorineural Hearing Loss

Otology and Neurotology

Otorhinolaryngology

Sensory Systems

English

Comprehensive Analysis of Deafness Genes in Families With Autosomal Recessive Nonsyndromic Hearing Loss

Multidisciplinary

English

Novel PTPRQ Mutations Identified in Three Congenital Hearing Loss Patients With Various Types of Hearing Loss

Annals of Otology, Rhinology and Laryngology

Otorhinolaryngology

English

Myo1c Mutations Associated With Hearing Loss Cause Defects in the Interaction With Nucleotide and Actin

Cellular and Molecular Life Sciences

Molecular Neuroscience

Molecular Medicine

Molecular Biology

English