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Genomics|September 15, 1996
Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1BZ Y Chen, T Hasson, P M Kelley, et al.Cytogenetics and Cell Genetics|January 1, 1997
Detailed map of a region commonly amplified at 11q13-->q14 in human breast carcinomaS Bekri, J Adélaïde, S Merscher, 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.Genomics|February 15, 1997
The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A)P M Kelley, M D Weston, Z Y Chen, 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 alleleR Varga, M R Avenarius, P M Kelley, et al.American Journal of Human Genetics|November 1, 1996
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patientsM D Weston, P M Kelley, L D Overbeck, et al.Genomics|July 1, 1996
The construction of a yeast artificial chromosome (YAC) contig in the vicinity of the Usher syndrome type IIa (USH2A) gene in 1q41J Sumegi, J Y Wang, D K Zhen, et al.The American Journal of Tropical Medicine and Hygiene|June 5, 2001
An outbreak of fulminant hepatitis delta in the Waorani, an indigenous people of the Amazon basin of EcuadorS R Manock, P M Kelley, K C Hyams, et al.Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.Pageof 5