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Lucinda Freeman

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Clinical Dysmorphology|June 11, 2008
Pfeiffer syndrome with neonatal death secondary to tracheal obstruction owing to the FGFR2 Glu565Ala mutationLucinda Freeman, George Elakis, Geoff Watson, et al.
NPJ Genomic Medicine|July 31, 2023
Scaling-up and future sustainability of a national reproductive genetic carrier screening programZoe Fehlberg, Stephanie Best, Janet C Long, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 16, 2022
Correspondence on "Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)" by Gregg et alSarah Righetti, Lisa Dive, Alison D Archibald, et al.
European Journal of Human Genetics : EJHG|August 22, 2025
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementationMichael P Mackley, Pankaj B Agrawal, Sara S Ali, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 6, 2016
A Pilot Randomized Controlled Trial of the Feasibility, Acceptability, and Impact of Giving Information on Personalized Genomic Risk of Melanoma to the PublicAmelia K Smit, David Espinoza, Ainsley J Newson, et al.
BMJ Open|June 16, 2026
Developing general practitioner and consumer supports for genomics in Australian primary care: a mixed-methods protocolJanet C Long, Alison D Archibald, Klay Lamprell, et al.
Atherosclerosis. Supplements|September 16, 2011
Familial hypercholesterolaemia: a model of care for AustralasiaGerald F Watts, David R Sullivan, Nicola Poplawski, et al.
Journal of Personalized Medicine|December 29, 2022
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and ImplementationAlison D Archibald, Belinda J McClaren, Jade Caruana, et al.
The New England Journal of Medicine|November 20, 2024
Nationwide, Couple-Based Genetic Carrier ScreeningEdwin P Kirk, Martin B Delatycki, Alison D Archibald, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Clinical Dysmorphology|June 11, 2008
Pfeiffer syndrome with neonatal death secondary to tracheal obstruction owing to the FGFR2 Glu565Ala mutationLucinda Freeman, George Elakis, Geoff Watson, et al.
NPJ Genomic Medicine|July 31, 2023
Scaling-up and future sustainability of a national reproductive genetic carrier screening programZoe Fehlberg, Stephanie Best, Janet C Long, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 16, 2022
Correspondence on "Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)" by Gregg et alSarah Righetti, Lisa Dive, Alison D Archibald, et al.
European Journal of Human Genetics : EJHG|August 22, 2025
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementationMichael P Mackley, Pankaj B Agrawal, Sara S Ali, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 6, 2016
A Pilot Randomized Controlled Trial of the Feasibility, Acceptability, and Impact of Giving Information on Personalized Genomic Risk of Melanoma to the PublicAmelia K Smit, David Espinoza, Ainsley J Newson, et al.
BMJ Open|June 16, 2026
Developing general practitioner and consumer supports for genomics in Australian primary care: a mixed-methods protocolJanet C Long, Alison D Archibald, Klay Lamprell, et al.
Atherosclerosis. Supplements|September 16, 2011
Familial hypercholesterolaemia: a model of care for AustralasiaGerald F Watts, David R Sullivan, Nicola Poplawski, et al.
Journal of Personalized Medicine|December 29, 2022
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and ImplementationAlison D Archibald, Belinda J McClaren, Jade Caruana, et al.
The New England Journal of Medicine|November 20, 2024
Nationwide, Couple-Based Genetic Carrier ScreeningEdwin P Kirk, Martin B Delatycki, Alison D Archibald, et al.
Pageof 3