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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.Clinical Genetics|April 22, 2004
Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosisA E Nisselle, M B Delatycki, V Collins, et al.Journal of Neurology|October 14, 2009
A comparison of three measures of upper limb function in Friedreich ataxiaL A Corben, G Tai, C Wilson, et al.Journal of Medical Ethics|November 5, 2005
Ethical considerations in presymptomatic testing for variant CJDR E Duncan, M B Delatycki, S J Collins, et al.Journal of Medical Genetics|May 5, 1999
Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissectionM B Delatycki, L Voullaire, D Francis, et al.Neuroscience|September 18, 2012
Binaural speech processing in individuals with auditory neuropathyG Rance, M M Ryan, P Carew, et al.Brain Research|July 10, 2012
A functional MRI study of motor dysfunction in Friedreich's ataxiaH Akhlaghi, L Corben, N Georgiou-Karistianis, et al.Clinical Genetics|November 17, 2009
SMARCB1/INI1 maternal germ line mosaicism in schwannomatosisT J M Hulsebos, S B Kenter, M E Jakobs, et al.Neuroscience|September 19, 2009
Mutant torsinA interacts with tyrosine hydroxylase in cultured cellsC A O'Farrell, K L Martin, M Hutton, et al.Pageof 12