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M B Delatycki

Showing results (51-60 of 58) with videos related to

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American Journal of Medical Genetics|October 26, 1999
Clinical and genetic study of Friedreich ataxia in an Australian populationM B Delatycki, D B Paris, R J Gardner, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2005
Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG geneM C Fahey, M A Knight, J H Shaw, et al.
Clinical Genetics|November 26, 2009
Implementation of ironXS: a study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schoolsM B Delatycki, M Wolthuizen, V Collins, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa-Kuroki) syndromeS M White, E M Thompson, A Kidd, 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.
Lancet (London, England)|July 26, 2005
Use of community genetic screening to prevent HFE-associated hereditary haemochromatosisM B Delatycki, K J Allen, A E Nisselle, et al.
Neurogastroenterology and Motility|May 22, 2018
Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo-obstructionG Ravenscroft, S Pannell, G O'Grady, et al.
European Journal of Medical Genetics|July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory servicesC A Stutterd, A Vanderver, P J Lockhart, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
American Journal of Medical Genetics|October 26, 1999
Clinical and genetic study of Friedreich ataxia in an Australian populationM B Delatycki, D B Paris, R J Gardner, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2005
Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG geneM C Fahey, M A Knight, J H Shaw, et al.
Clinical Genetics|November 26, 2009
Implementation of ironXS: a study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schoolsM B Delatycki, M Wolthuizen, V Collins, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa-Kuroki) syndromeS M White, E M Thompson, A Kidd, 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.
Lancet (London, England)|July 26, 2005
Use of community genetic screening to prevent HFE-associated hereditary haemochromatosisM B Delatycki, K J Allen, A E Nisselle, et al.
Neurogastroenterology and Motility|May 22, 2018
Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo-obstructionG Ravenscroft, S Pannell, G O'Grady, et al.
European Journal of Medical Genetics|July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory servicesC A Stutterd, A Vanderver, P J Lockhart, et al.
Pageof 6