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Gareth Baynam

Showing results (21-30 of 178) with videos related to

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Frontiers in Pediatrics|August 4, 2022
Editorial: Congenital anomalies: State of the art and the new paradigms for a precision public health approachBabak Khoshnood, Gareth Baynam, Maria Loane, et al.
European Journal of Human Genetics : EJHG|February 17, 2018
Incidental inequityKristen J Nowak, Alicia Bauskis, Hugh J Dawkins, et al.
Paediatric and Perinatal Epidemiology|May 5, 2023
Trends in prenatal diagnosis of congenital anomalies in Western Australia between 1980 and 2020: A population-based studyCassandra MacArthur, Michele Hansen, Gareth Baynam, et al.
Personalized Medicine|June 4, 2021
Ethics and equity in rare disease research and healthcareMaria Koromina, Vasileios Fanaras, Gareth Baynam, et al.
Frontiers in Pediatrics|November 29, 2023
Surfacing undiagnosed disease: consideration, counting and codingMegan F Baxter, Michele Hansen, Dylan Gration, et al.
Pharmaceutical Medicine|July 8, 2024
Increasing Diversity, Equity, Inclusion, and Accessibility in Rare Disease Clinical TrialsGareth Baynam, Simeón Baker, Charles Steward, et al.
Early Human Development|December 29, 2024
Neurodevelopmental impairment in children with Robin sequence: A systematic review and meta-analysisDimple Goel, Andrew Wilson, Gareth Baynam, et al.
Children (Basel, Switzerland)|May 28, 2022
Medical Comorbidities in <i>MECP2</i> Duplication Syndrome: Results from the International <i>MECP2</i> Duplication DatabaseDaniel Ta, Jenny Downs, Gareth Baynam, et al.
Orphanet Journal of Rare Diseases|April 8, 2026
TrialR: critical enablers and the need for reusable Rare Disease Clinical Trial infrastructure in Western AustraliaBradley MacDonald, Maddison Burmaz, Sue Baker, et al.
Orphanet Journal of Rare Diseases|March 22, 2022
A brief history of MECP2 duplication syndrome: 20-years of clinical understandingDaniel Ta, Jenny Downs, Gareth Baynam, et al.
Pageof 18

Showing results (21-30 of 178) with videos related to

Sort By:
Pageof 18
Frontiers in Pediatrics|August 4, 2022
Editorial: Congenital anomalies: State of the art and the new paradigms for a precision public health approachBabak Khoshnood, Gareth Baynam, Maria Loane, et al.
European Journal of Human Genetics : EJHG|February 17, 2018
Incidental inequityKristen J Nowak, Alicia Bauskis, Hugh J Dawkins, et al.
Paediatric and Perinatal Epidemiology|May 5, 2023
Trends in prenatal diagnosis of congenital anomalies in Western Australia between 1980 and 2020: A population-based studyCassandra MacArthur, Michele Hansen, Gareth Baynam, et al.
Personalized Medicine|June 4, 2021
Ethics and equity in rare disease research and healthcareMaria Koromina, Vasileios Fanaras, Gareth Baynam, et al.
Frontiers in Pediatrics|November 29, 2023
Surfacing undiagnosed disease: consideration, counting and codingMegan F Baxter, Michele Hansen, Dylan Gration, et al.
Pharmaceutical Medicine|July 8, 2024
Increasing Diversity, Equity, Inclusion, and Accessibility in Rare Disease Clinical TrialsGareth Baynam, Simeón Baker, Charles Steward, et al.
Early Human Development|December 29, 2024
Neurodevelopmental impairment in children with Robin sequence: A systematic review and meta-analysisDimple Goel, Andrew Wilson, Gareth Baynam, et al.
Children (Basel, Switzerland)|May 28, 2022
Medical Comorbidities in <i>MECP2</i> Duplication Syndrome: Results from the International <i>MECP2</i> Duplication DatabaseDaniel Ta, Jenny Downs, Gareth Baynam, et al.
Orphanet Journal of Rare Diseases|April 8, 2026
TrialR: critical enablers and the need for reusable Rare Disease Clinical Trial infrastructure in Western AustraliaBradley MacDonald, Maddison Burmaz, Sue Baker, et al.
Orphanet Journal of Rare Diseases|March 22, 2022
A brief history of MECP2 duplication syndrome: 20-years of clinical understandingDaniel Ta, Jenny Downs, Gareth Baynam, et al.
Pageof 18