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Journal of Human Genetics|March 17, 2009
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in PakistanisSaima Anwar, Saima Riazuddin, Zubair M Ahmed, et al.Blood|June 14, 2000
Posttranscriptional cell cycle-dependent regulation of human FANCC expressionM C Heinrich, K V Silvey, S Stone, et al.Schizophrenia Research|August 1, 1993
Neurophysiological and neuropsychological evidence for attentional dysfunction in schizophreniaC M Cullum, J G Harris, M C Waldo, et al.Society of Reproduction and Fertility Supplement|May 12, 2007
Judge, jury and executioner: the auto-regulation of luteal functionG D Niswender, T L Davis, R J Griffith, et al.Journal of Medical Genetics|August 3, 2004
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunctionS Naz, A J Griffith, S Riazuddin, et al.Transplantation|October 1, 1990
Cyclosporine nephrotoxicity in cardiac allograft patients--a seven-year follow-upA Greenberg, M E Thompson, B J Griffith, et al.The Journal of Biological Chemistry|September 12, 2020
Expression of a TMC6-TMC8-CIB1 heterotrimeric complex in lymphocytes is regulated by each of the componentsChuan-Jin Wu, Xing Li, Connie L Sommers, et al.The Journal of Biological Chemistry|March 10, 1985
Structural and functional characteristics of activated human factor IX after chemical modification of gamma-carboxyglutamic acid residuesD L Straight, G B Sherrill, C M Noyes, et al.BMC Public Health|June 11, 2024
"It's another gay disease": an intersectional qualitative approach contextualizing the lived experiences of young gay, bisexual, and other sexual minoritized men in the United States during the mpox outbreakBryce Puesta Takenaka, Sally J Kirklewski, Frances J Griffith, et al.BMC Medical Genetics|July 4, 2019
SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueductJanet R Chao, Parna Chattaraj, Tina Munjal, et al.Pageof 68