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Lilian Downie

Showing results (1-10 of 46) with videos related to

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Australian Family Physician|April 5, 2017
Advances in genomic testingSarah Donoghue, Lilian Downie, Chloe Stutterd
Journal of Paediatrics and Child Health|December 31, 2013
Congenital chylothorax: associations and neonatal outcomesLilian Downie, Arun Sasi, Atul Malhotra
American Journal of Medical Genetics. Part A|August 14, 2023
An incidental finding in prenatal exome sequencing-A case study and review of the clinical and ethical considerationsIgnatius Rudd, Gulvir Gill, Michael Buckley, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|March 26, 2025
Insights and Experiences From the 'Gatekeepers': A Qualitative Study Exploring Clinician Perspectives on Providing Publicly Funded Prenatal Exome SequencingSamantha Dayman, Melissa Graetz, Lisa Hui, et al.
JAMA Network Open|July 20, 2021
Principles of Genomic Newborn Screening Programs: A Systematic ReviewLilian Downie, Jane Halliday, Sharon Lewis, et al.
Prenatal Diagnosis|August 8, 2023
Prenatal diagnosis of cleft lip and/or palate: What do we tell prospective parents?Courtney Wilkes, Melissa Graetz, Lilian Downie, et al.
American Journal of Medical Genetics. Part A|June 29, 2021
Personal utility of genomic sequencing for infants with congenital deafnessErin Tutty, David J Amor, Anna Jarmolowicz, et al.
Archives of Disease in Childhood|November 13, 2012
Community-acquired neonatal and infant sepsis in developing countries: efficacy of WHO's currently recommended antibiotics--systematic review and meta-analysisLilian Downie, Raffaela Armiento, Rami Subhi, et al.
The Laryngoscope|December 31, 2020
Exome Sequencing for Isolated Congenital Hearing Loss: A Cost-Effectiveness AnalysisLilian Downie, David J Amor, Jane Halliday, et al.
Case Reports in Genetics|March 21, 2014
Monosomy 21 seen in live born is unlikely to represent true monosomy 21: a case report and review of the literatureTrent Burgess, Lilian Downie, Mark D Pertile, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Australian Family Physician|April 5, 2017
Advances in genomic testingSarah Donoghue, Lilian Downie, Chloe Stutterd
Journal of Paediatrics and Child Health|December 31, 2013
Congenital chylothorax: associations and neonatal outcomesLilian Downie, Arun Sasi, Atul Malhotra
American Journal of Medical Genetics. Part A|August 14, 2023
An incidental finding in prenatal exome sequencing-A case study and review of the clinical and ethical considerationsIgnatius Rudd, Gulvir Gill, Michael Buckley, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|March 26, 2025
Insights and Experiences From the 'Gatekeepers': A Qualitative Study Exploring Clinician Perspectives on Providing Publicly Funded Prenatal Exome SequencingSamantha Dayman, Melissa Graetz, Lisa Hui, et al.
JAMA Network Open|July 20, 2021
Principles of Genomic Newborn Screening Programs: A Systematic ReviewLilian Downie, Jane Halliday, Sharon Lewis, et al.
Prenatal Diagnosis|August 8, 2023
Prenatal diagnosis of cleft lip and/or palate: What do we tell prospective parents?Courtney Wilkes, Melissa Graetz, Lilian Downie, et al.
American Journal of Medical Genetics. Part A|June 29, 2021
Personal utility of genomic sequencing for infants with congenital deafnessErin Tutty, David J Amor, Anna Jarmolowicz, et al.
Archives of Disease in Childhood|November 13, 2012
Community-acquired neonatal and infant sepsis in developing countries: efficacy of WHO's currently recommended antibiotics--systematic review and meta-analysisLilian Downie, Raffaela Armiento, Rami Subhi, et al.
The Laryngoscope|December 31, 2020
Exome Sequencing for Isolated Congenital Hearing Loss: A Cost-Effectiveness AnalysisLilian Downie, David J Amor, Jane Halliday, et al.
Case Reports in Genetics|March 21, 2014
Monosomy 21 seen in live born is unlikely to represent true monosomy 21: a case report and review of the literatureTrent Burgess, Lilian Downie, Mark D Pertile, et al.
Pageof 5