Showing results (131-140 of 138) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 138 results.
Brain : a Journal of Neurology|April 1, 1987
The role of insulin resistance in the pathogenesis of myotonic muscular dystrophyA J Hudson, M W Huff, C G Wright, et al.
American Journal of Otolaryngology|May 1, 1982
A calcareous concretion in the posterior semicircular duct of a human labyrinthC G Wright, R C Rouse, G H Zajic, et al.
American Journal of Medical Genetics|October 1, 1984
A "new" lethal multiple congenital anomaly syndrome: joint contractures, cerebellar hypoplasia, renal hypoplasia, urogenital anomalies, tongue cysts, shortness of limbs, eye abnormalities, defects of the heart, gallbladder agenesis, and ear malformationsJ C Rutledge, J M Friedman, M J Harrod, et al.
Nature Genetics|January 4, 2001
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin geneK N Alagramam, C L Murcia, H Y Kwon, et al.
Science (New York, N.Y.)|January 24, 1986
A balanced translocation in mice with a neurological defectJ C Rutledge, K T Cain, N L Cacheiro, et al.
Hearing Research|September 9, 2000
Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzerK N Alagramam, J Zahorsky-Reeves, C G Wright, et al.
Genetics|August 3, 1999
A new mouse insertional mutation that causes sensorineural deafness and vestibular defectsK N Alagramam, H Y Kwon, N L Cacheiro, et al.
Hearing Research|August 5, 2006
A new spontaneous mutation in the mouse protocadherin 15 geneQ Y Zheng, H Yu, J L Washington, et al.
Pageof 14