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Neurology
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May 29, 2025
Haemochromatosis Genotypes and Incident Dementia in a Prospective Study of Older Adults
Chenglong Yu, Martin Delatycki, Sultana Monira Hussain, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
September 29, 2009
Population-based carrier screening for cystic fibrosis in Victoria: the first three years experience
John Massie, Vicki Petrou, Robyn Forbes, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
December 1, 2023
Endophenotyping social cognition in the broader autism phenotype
Emmanuel Peng Kiat Pua, Tarishi Desai, Cherie Green, et al.
Neurology. Genetics
|
October 3, 2022
Overview of the Clinical Approach to Individuals With Cerebellar Ataxia and Neuropathy
Leslie J Roberts, Michael McVeigh, Linda Seiderer, et al.
European Journal of Human Genetics : EJHG
|
November 2, 2021
Development and use of the Australian reproductive genetic carrier screening decision aid
Emily King, Jane Halliday, Alison D Archibald, et al.
BMC Medical Ethics
|
May 22, 2021
Study protocol: the Australian genetics and life insurance moratorium-monitoring the effectiveness and response (A-GLIMMER) project
Jane Tiller, Aideen McInerney-Leo, Andrea Belcher, et al.
Annals of Clinical and Translational Neurology
|
September 15, 2017
Impact of diabetes in the Friedreich ataxia clinical outcome measures study
Ashley McCormick, Jennifer Farmer, Susan Perlman, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2003
Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotype
Linda S Weaving, Sarah L Williamson, Bruce Bennetts, et al.
Human Mutation
|
April 2, 2009
GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype
William A Paznekas, Barbara Karczeski, Sascha Vermeer, et al.
Annals of Clinical and Translational Neurology
|
January 4, 2018
Neuropathology of childhood-onset basal ganglia degeneration caused by mutation of <i>VAC14</i>
Chloe Stutterd, Peter Diakumis, Melanie Bahlo, et al.
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of 6
Search research articles
Search
Showing results (21-30 of 57) with videos related to
Sort By:
Page
of 6
Neurology
|
May 29, 2025
Haemochromatosis Genotypes and Incident Dementia in a Prospective Study of Older Adults
Chenglong Yu, Martin Delatycki, Sultana Monira Hussain, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
September 29, 2009
Population-based carrier screening for cystic fibrosis in Victoria: the first three years experience
John Massie, Vicki Petrou, Robyn Forbes, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
December 1, 2023
Endophenotyping social cognition in the broader autism phenotype
Emmanuel Peng Kiat Pua, Tarishi Desai, Cherie Green, et al.
Neurology. Genetics
|
October 3, 2022
Overview of the Clinical Approach to Individuals With Cerebellar Ataxia and Neuropathy
Leslie J Roberts, Michael McVeigh, Linda Seiderer, et al.
European Journal of Human Genetics : EJHG
|
November 2, 2021
Development and use of the Australian reproductive genetic carrier screening decision aid
Emily King, Jane Halliday, Alison D Archibald, et al.
BMC Medical Ethics
|
May 22, 2021
Study protocol: the Australian genetics and life insurance moratorium-monitoring the effectiveness and response (A-GLIMMER) project
Jane Tiller, Aideen McInerney-Leo, Andrea Belcher, et al.
Annals of Clinical and Translational Neurology
|
September 15, 2017
Impact of diabetes in the Friedreich ataxia clinical outcome measures study
Ashley McCormick, Jennifer Farmer, Susan Perlman, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2003
Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotype
Linda S Weaving, Sarah L Williamson, Bruce Bennetts, et al.
Human Mutation
|
April 2, 2009
GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype
William A Paznekas, Barbara Karczeski, Sascha Vermeer, et al.
Annals of Clinical and Translational Neurology
|
January 4, 2018
Neuropathology of childhood-onset basal ganglia degeneration caused by mutation of <i>VAC14</i>
Chloe Stutterd, Peter Diakumis, Melanie Bahlo, et al.
Page
of 6