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Journal of Genetic Counseling
|
July 15, 2021
Genetic counselors and legal recognition: A made-for-Canada approach
Deborah M Lambert, Dimitri Patrinos, Bartha Maria Knoppers, et al.
European Journal of Human Genetics : EJHG
|
December 2, 2020
Reply to E. Vicente et al
Ana Rath, Deborah M Lambert, Annie Olry, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2025
An Additional Report of a Female With a Complex XY Translocation Is Presented Who Has Successfully Completed a Pregnancy With Significant Y Chromosome Material Gain and Partial X Deletion
John Coleman, Nicola Walsh, Deborah M Lambert, et al.
Journal of Community Genetics
|
July 3, 2021
Fatal fetal abnormality Irish live-born survival-an observational study
Emer Gunne, Sally Ann Lynch, Cliona McGarvey, et al.
Orphanet Journal of Rare Diseases
|
November 5, 2020
A retrospective review of the contribution of rare diseases to paediatric mortality in Ireland
Emer Gunne, Cliona McGarvey, Karina Hamilton, et al.
European Journal of Human Genetics : EJHG
|
July 19, 2022
An estimate of the cumulative paediatric prevalence of rare diseases in Ireland and comment on the literature
Emer Gunne, Deborah M Lambert, Alana J Ward, et al.
Molecular Medicine Reports
|
April 8, 2011
Novel ETHE1 mutation in a carrier couple having prior offspring affected with ethylmalonic encephalopathy: Genetic analysis, clinical management and reproductive outcome
David J Walsh, Eric S Sills, Deborah M Lambert, et al.
BMC Medical Genetics
|
December 6, 2005
Polymorphisms of the Flavin containing monooxygenase 3 (FMO3) gene do not predispose to essential hypertension in Caucasians
Ciara Dolan, Denis C Shields, Alice Stanton, et al.
European Journal of Human Genetics : EJHG
|
September 19, 2019
Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database
Stéphanie Nguengang Wakap, Deborah M Lambert, Annie Olry, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2017
Incidence of Fragile X syndrome in Ireland
James J O'Byrne, Michael Sweeney, Deirdre E Donnelly, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Journal of Genetic Counseling
|
July 15, 2021
Genetic counselors and legal recognition: A made-for-Canada approach
Deborah M Lambert, Dimitri Patrinos, Bartha Maria Knoppers, et al.
European Journal of Human Genetics : EJHG
|
December 2, 2020
Reply to E. Vicente et al
Ana Rath, Deborah M Lambert, Annie Olry, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2025
An Additional Report of a Female With a Complex XY Translocation Is Presented Who Has Successfully Completed a Pregnancy With Significant Y Chromosome Material Gain and Partial X Deletion
John Coleman, Nicola Walsh, Deborah M Lambert, et al.
Journal of Community Genetics
|
July 3, 2021
Fatal fetal abnormality Irish live-born survival-an observational study
Emer Gunne, Sally Ann Lynch, Cliona McGarvey, et al.
Orphanet Journal of Rare Diseases
|
November 5, 2020
A retrospective review of the contribution of rare diseases to paediatric mortality in Ireland
Emer Gunne, Cliona McGarvey, Karina Hamilton, et al.
European Journal of Human Genetics : EJHG
|
July 19, 2022
An estimate of the cumulative paediatric prevalence of rare diseases in Ireland and comment on the literature
Emer Gunne, Deborah M Lambert, Alana J Ward, et al.
Molecular Medicine Reports
|
April 8, 2011
Novel ETHE1 mutation in a carrier couple having prior offspring affected with ethylmalonic encephalopathy: Genetic analysis, clinical management and reproductive outcome
David J Walsh, Eric S Sills, Deborah M Lambert, et al.
BMC Medical Genetics
|
December 6, 2005
Polymorphisms of the Flavin containing monooxygenase 3 (FMO3) gene do not predispose to essential hypertension in Caucasians
Ciara Dolan, Denis C Shields, Alice Stanton, et al.
European Journal of Human Genetics : EJHG
|
September 19, 2019
Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database
Stéphanie Nguengang Wakap, Deborah M Lambert, Annie Olry, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2017
Incidence of Fragile X syndrome in Ireland
James J O'Byrne, Michael Sweeney, Deirdre E Donnelly, et al.
Page
of 2