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Journal of Neurology
|
March 14, 2009
Evaluating the progression of Friedreich ataxia and its treatment
Martin B Delatycki
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
July 22, 2008
Population screening for reproductive risk for single gene disorders in Australia: now and the future
Martin B Delatycki
Pathology
|
December 27, 2011
The ethics of screening for disease
Martin B Delatycki
European Journal of Human Genetics : EJHG
|
October 7, 2018
Presymptomatic testing of those at 25% risk of autosomal dominant neurodegenerative disease- testing team beware
Martin B Delatycki
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
March 8, 2005
A de novo, apparently balanced reciprocal translocation in a child with developmental delay whose mother was being treated with low-dose methotrexate at the time of conception
Martin B Delatycki
Journal of Medical Ethics
|
June 16, 2021
Genetic discrimination in life insurance: a human rights issue
Jane Tiller, Martin B Delatycki
Paediatric Respiratory Reviews
|
March 8, 2013
Cystic fibrosis carrier screening
John Massie, Martin B Delatycki
Neurology
|
June 24, 2016
Huntington disease: More common than you think?
Martin B Delatycki, Oliver Bandmann
Journal of Child Neurology
|
July 4, 2012
Clinical features of Friedreich ataxia
Martin B Delatycki, Louise A Corben
Genes
|
August 29, 2024
Population Screening for Hereditary Haemochromatosis-Should It Be Carried Out, and If So, How?
Martin B Delatycki, Katrina J Allen
Page
of 35
Search research articles
Search
Showing results (1-10 of 346) with videos related to
Sort By:
Page
of 35
Journal of Neurology
|
March 14, 2009
Evaluating the progression of Friedreich ataxia and its treatment
Martin B Delatycki
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
July 22, 2008
Population screening for reproductive risk for single gene disorders in Australia: now and the future
Martin B Delatycki
Pathology
|
December 27, 2011
The ethics of screening for disease
Martin B Delatycki
European Journal of Human Genetics : EJHG
|
October 7, 2018
Presymptomatic testing of those at 25% risk of autosomal dominant neurodegenerative disease- testing team beware
Martin B Delatycki
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
March 8, 2005
A de novo, apparently balanced reciprocal translocation in a child with developmental delay whose mother was being treated with low-dose methotrexate at the time of conception
Martin B Delatycki
Journal of Medical Ethics
|
June 16, 2021
Genetic discrimination in life insurance: a human rights issue
Jane Tiller, Martin B Delatycki
Paediatric Respiratory Reviews
|
March 8, 2013
Cystic fibrosis carrier screening
John Massie, Martin B Delatycki
Neurology
|
June 24, 2016
Huntington disease: More common than you think?
Martin B Delatycki, Oliver Bandmann
Journal of Child Neurology
|
July 4, 2012
Clinical features of Friedreich ataxia
Martin B Delatycki, Louise A Corben
Genes
|
August 29, 2024
Population Screening for Hereditary Haemochromatosis-Should It Be Carried Out, and If So, How?
Martin B Delatycki, Katrina J Allen
Page
of 35