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Deborah M Lambert

Showing results (1-10 of 14) with videos related to

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Journal of Genetic Counseling|July 15, 2021
Genetic counselors and legal recognition: A made-for-Canada approachDeborah M Lambert, Dimitri Patrinos, Bartha Maria Knoppers, et al.
European Journal of Human Genetics : EJHG|December 2, 2020
Reply to E. Vicente et alAna 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 DeletionJohn Coleman, Nicola Walsh, Deborah M Lambert, et al.
Journal of Community Genetics|July 3, 2021
Fatal fetal abnormality Irish live-born survival-an observational studyEmer 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 IrelandEmer 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 literatureEmer 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 outcomeDavid 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 CaucasiansCiara 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 databaseStéphanie 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 IrelandJames J O'Byrne, Michael Sweeney, Deirdre E Donnelly, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Journal of Genetic Counseling|July 15, 2021
Genetic counselors and legal recognition: A made-for-Canada approachDeborah M Lambert, Dimitri Patrinos, Bartha Maria Knoppers, et al.
European Journal of Human Genetics : EJHG|December 2, 2020
Reply to E. Vicente et alAna 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 DeletionJohn Coleman, Nicola Walsh, Deborah M Lambert, et al.
Journal of Community Genetics|July 3, 2021
Fatal fetal abnormality Irish live-born survival-an observational studyEmer 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 IrelandEmer 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 literatureEmer 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 outcomeDavid 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 CaucasiansCiara 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 databaseStéphanie 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 IrelandJames J O'Byrne, Michael Sweeney, Deirdre E Donnelly, et al.
Pageof 2