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M B Delatycki

Showing results (41-50 of 58) with videos related to

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Journal of Medical Genetics|September 11, 1998
Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA geneM B Delatycki, D Paris, R J Gardner, et al.
Clinical Genetics|July 6, 2010
Evaluation of a multi-disease carrier screening programme in Ashkenazi Jewish high schoolsL Ioannou, J Massie, S Lewis, et al.
Journal of Medical Genetics|June 1, 1997
A maternally transmitted lethal neonatal progeroid syndrome with prominent genitourinary and gastrointestinal featuresM B Delatycki, M A Cleary, A Bankier, et al.
European Journal of Neurology|August 28, 2007
Quality of life in Friedreich ataxia: what clinical, social and demographic factors are important?C L Wilson, M C Fahey, L A Corben, et al.
Neurogenetics|March 25, 2000
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA geneS M Forrest, M Knight, M B Delatycki, et al.
Brain and Cognition|March 1, 2011
Impaired inhibition of prepotent motor tendencies in Friedreich ataxia demonstrated by the Simon interference taskL A Corben, H Akhlaghi, N Georgiou-Karistianis, et al.
Journal of Medical Genetics|February 5, 2003
A novel pericentric inversion of chromosome 3 cosegregates with a developmental-behavioural phenotypeD Efron, M B Delatycki, M G de Silva, et al.
Clinical Genetics|January 26, 2006
Educational outcomes of a workplace screening program for genetic susceptibility to hemochromatosisA E Nisselle, V R Collins, A A Gason, et al.
Clinical Genetics|April 22, 2004
A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosisM B Delatycki, K J Allen, P Gow, et al.
Heart, Lung & Circulation|December 6, 2016
A Novel Mechanism for Human Cardiac Ankyrin-B Syndrome due to Reciprocal Chromosomal TranslocationA J Huq, M D Pertile, A M Davis, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|September 11, 1998
Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA geneM B Delatycki, D Paris, R J Gardner, et al.
Clinical Genetics|July 6, 2010
Evaluation of a multi-disease carrier screening programme in Ashkenazi Jewish high schoolsL Ioannou, J Massie, S Lewis, et al.
Journal of Medical Genetics|June 1, 1997
A maternally transmitted lethal neonatal progeroid syndrome with prominent genitourinary and gastrointestinal featuresM B Delatycki, M A Cleary, A Bankier, et al.
European Journal of Neurology|August 28, 2007
Quality of life in Friedreich ataxia: what clinical, social and demographic factors are important?C L Wilson, M C Fahey, L A Corben, et al.
Neurogenetics|March 25, 2000
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA geneS M Forrest, M Knight, M B Delatycki, et al.
Brain and Cognition|March 1, 2011
Impaired inhibition of prepotent motor tendencies in Friedreich ataxia demonstrated by the Simon interference taskL A Corben, H Akhlaghi, N Georgiou-Karistianis, et al.
Journal of Medical Genetics|February 5, 2003
A novel pericentric inversion of chromosome 3 cosegregates with a developmental-behavioural phenotypeD Efron, M B Delatycki, M G de Silva, et al.
Clinical Genetics|January 26, 2006
Educational outcomes of a workplace screening program for genetic susceptibility to hemochromatosisA E Nisselle, V R Collins, A A Gason, et al.
Clinical Genetics|April 22, 2004
A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosisM B Delatycki, K J Allen, P Gow, et al.
Heart, Lung & Circulation|December 6, 2016
A Novel Mechanism for Human Cardiac Ankyrin-B Syndrome due to Reciprocal Chromosomal TranslocationA J Huq, M D Pertile, A M Davis, et al.
Pageof 6