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Journal of Chronic Diseases|January 1, 1984
Use of the one sample t-test in the real worldN A Cressie, L J Sheffield, H J WhitfordJournal of Neurology, Neurosurgery, and Psychiatry|October 24, 2006
How is disease progress in Friedreich's ataxia best measured? A study of four rating scalesM C Fahey, L Corben, V Collins, et al.American Journal of Medical Genetics|November 15, 1992
Fragile X family with unusual digital and facial abnormalities, cleft lip and palate, and epilepsyD Z Loesch, D A Hay, L J SheffieldThe FEBS Journal|April 1, 2015
STAT3 the oncogene - still eluding therapy?Matthew S Wake, Christine J WatsonAmerican Journal of Medical Genetics|June 1, 1991
Two forms of ring 13 in a child with rhabdomyosarcomaL E Voullaire, V Petrovic, L J Sheffield, et al.American Journal of Medical Genetics|September 1, 1987
A genetic follow-up study of 64 patients with the Pierre Robin complexL J Sheffield, J A Reiss, K Strohm, et al.Human Genetics|October 30, 1999
G130V, a common FRDA point mutation, appears to have arisen from a common founderM B Delatycki, M Knight, M Koenig, et al.Reproductive Biomedicine Online|January 16, 2019
Germ cell arrest associated with aSETX mutation in ataxia oculomotor apraxia type 2S R Catford, M K O'Bryan, R I McLachlan, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 1993
An ultrasound renal cyst prevalence survey: specificity data for inherited renal cystic diseasesD Ravine, R N Gibson, J Donlan, et al.Pageof 662