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Archives of Otolaryngology--Head & Neck Surgery|September 1, 1991
Autosomal dominant sensorineural hearing loss. Pedigrees, audiologic findings, and temporal bone findings in two kindredsU Khetarpal, H F Schuknecht, R R Gacek, et al.
Hearing Research|September 1, 1994
Expression and localization of COL2A1 mRNA and type II collagen in human fetal cochleaU Khetarpal, N G Robertson, T J Yoo, et al.
Genomics|September 1, 1994
Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screeningN G Robertson, U Khetarpal, G A Gutiérrez-Espeleta, et al.
Human Mutation|January 1, 1997
Norrie disease gene mutation in a large Costa Rican kindred with a novel phenotype including venous insufficiencyH L Rehm, G A Gutiérrez-Espeleta, R Garcia, et al.
Human Molecular Genetics|July 1, 1996
A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13E N Manolis, N Yandavi, J B Nadol, et al.
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