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Publications by Christina M. Sloan
Novel PTPRQ Mutations Identified in Three Congenital Hearing Loss Patients With Various Types of Hearing Loss
Annals of Otology, Rhinology and Laryngology
Medicine
Otorhinolaryngology
Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation
Annals of Otology, Rhinology and Laryngology
Medicine
Otorhinolaryngology
Related publications
Hearing Loss in Congenital Microtia
Congenital Hearing Loss in Down Syndrome
Journal of Pediatrics
Child Health
Pediatrics
Perinatology
USH2A Mutations Identified by Massively Parallel Sequencing in 3 Children With Sensorineural Hearing Loss
AUDIOLOGY JAPAN
Hearing Outcome of Patients With Acute Noise-Induced Hearing Loss
Korean Journal of Otorhinolaryngology-Head and Neck Surgery
A C-Terminal Nonsense Mutation Links PTPRQ With Autosomal-Dominant Hearing Loss, DFNA73
Genetics in Medicine
Medicine
Genetics
Molecular Analysis of Mitochondrial Gene Mutations in Korean Patients With Nonsyndromic Hearing Loss
International Journal of Molecular Medicine
Medicine
Genetics
Congenital Cytomegalovirus Infection and Sensorineural Hearing Loss
Practica Otologica, Supplement
Otorhinolaryngology
Vowel Production of Mandarin-Speaking Hearing Aid Users With Different Types of Hearing Loss
PLoS ONE
Multidisciplinary
Novel Recessive PDZD7 Biallelic Mutations in Two Chinese Families With Non-Syndromic Hearing Loss
American Journal of Medical Genetics, Part A
Genetics
