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Virology|January 9, 2001
The sequence and antiapoptotic functional domains of the human cytomegalovirus UL37 exon 1 immediate early protein are conserved in multiple primary strainsW A Hayajneh, A M Colberg-Poley, A Skaletskaya, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 14, 2010
Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in DrosophilaCynthia J Schoen, Sarah B Emery, Marc C Thorne, et al.
Journal of the Association for Research in Otolaryngology : JARO|January 28, 2005
A dominantly inherited progressive deafness affecting distal auditory nerve and hair cellsArnold Starr, Brandon Isaacson, Henry J Michalewski, et al.
American Journal of Human Genetics|June 29, 2002
Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding nogginDavid J Brown, Theresa B Kim, Elizabeth M Petty, et al.
Human Molecular Genetics|October 1, 1995
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3M M Lesperance, J W Hall, F H Bess, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 7, 2003
Characterization of a stapes ankylosis family with a NOG mutationDavid J Brown, Theresa B Kim, Elizabeth M Petty, et al.
Current Oncology (Toronto, Ont.)|June 4, 2020
Treatment of non-small-cell lung cancer after progression on nivolumab or pembrolizumabA T Freeman, M Lesperance, E S Wai, et al.
Journal of Pediatric Orthopedics|June 10, 2011
Ossifying lipoma of c1-c2 in an adolescentKyle C Bohm, Michael V Birman, Selina R Silva, et al.
American Journal of Medical Genetics. Part A|February 14, 2009
A novel chromosome 19p13.12 deletion in a child with multiple congenital anomaliesDaniel R Jensen, Donna M Martin, Stephen Gebarski, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Pure monosomy and pure trisomy of 13q21.2-31.1 consequent to a familial insertional translocation: exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1)Francesca R Grati, Marci M Lesperance, Simona De Toffol, et al.
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