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The American Journal of Otology
|
November 27, 1998
Tone burst auditory brain stem response latency estimates of cochlear travel time in Meniere's disease, cochlear hearing loss, and normal ears
J G Murray, E S Cohn, L A Harker, et al.
The American Journal of Occupational Therapy : Official Publication of the American Occupational Therapy Association
|
January 1, 1990
A part-time Level II fieldwork program
L A Adelstein, E S Cohn, R C Baker, et al.
Violence and Victims
|
March 30, 2007
Unwanted sexual contact on campus: a comparison of women's and men's experiences
Victoria L Banyard, S Ward, E S Cohn, et al.
Genetic Testing
|
February 24, 2001
The M34T allele variant of connexin 26
R A Cucci, S Prasad, P M Kelley, et al.
Pediatrics
|
March 2, 1999
Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)
E S Cohn, P M Kelley, T W Fowler, et al.
Journal of Medical Genetics
|
December 24, 2005
OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele
R Varga, M R Avenarius, P M Kelley, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 26) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 26 results.
The American Journal of Otology
|
November 27, 1998
Tone burst auditory brain stem response latency estimates of cochlear travel time in Meniere's disease, cochlear hearing loss, and normal ears
J G Murray, E S Cohn, L A Harker, et al.
The American Journal of Occupational Therapy : Official Publication of the American Occupational Therapy Association
|
January 1, 1990
A part-time Level II fieldwork program
L A Adelstein, E S Cohn, R C Baker, et al.
Violence and Victims
|
March 30, 2007
Unwanted sexual contact on campus: a comparison of women's and men's experiences
Victoria L Banyard, S Ward, E S Cohn, et al.
Genetic Testing
|
February 24, 2001
The M34T allele variant of connexin 26
R A Cucci, S Prasad, P M Kelley, et al.
Pediatrics
|
March 2, 1999
Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)
E S Cohn, P M Kelley, T W Fowler, et al.
Journal of Medical Genetics
|
December 24, 2005
OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele
R Varga, M R Avenarius, P M Kelley, et al.
Page
of 3