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Journal of Medical Genetics|June 1, 1997
The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1)R Morell, T B Friedman, J H Asher, et al.Irish Medical Journal|March 22, 2006
Prevalence of suboptimal vitamin D status in young, adult and elderly Irish subjectsT R Hill, A Flynn, M Kiely, et al.Human Molecular Genetics|July 11, 1992
A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian familyR Morell, T B Friedman, S Moeljopawiro, et al.Behavioural Brain Research|February 13, 2001
Reconsideration of the role of the hippocampus in learned inhibitionK H Chan, J R Morell, L E Jarrard, et al.Cureus|August 21, 2023
The Sex Data Gap Within Implantable Cardioverter Defibrillator (ICD) Studies: A Retrospective Study of Literature From 1980 Until 2022Peter M Magnusson, Kaitlyn R Morell, Jonelys Lazo, et al.Acta Endocrinologica|December 1, 1991
Course of thyroid iodine concentration during treatment of endemic goitre with iodine and a combination of iodine and levothyroxineB Saller, R Hoermann, M M Ritter, et al.Brain : a Journal of Neurology|September 1, 1979
Central core disease: clinical and pathological evidence of progression within a familyV H Patterson, T R Hill, P J Fletcher, et al.Journal of Cannabis Research|August 29, 2025
Water use and productivity of Cannabis sativa L., KwaZulu-Natal Midlands, South AfricaG M Denton, A Clulow, T R Hill, et al.Human Heredity|January 1, 1997
Three mutations in the paired homeodomain of PAX3 that cause Waardenburg syndrome type 1R Morell, M L Carey, A K Lalwani, et al.Genomics|June 15, 1996
Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability: a murine model of Waardenburg syndrome variationJ H Asher, R W Harrison, R Morell, et al.Pageof 5