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Gareth S Baynam

Showing results (1-10 of 18) with videos related to

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The Medical Journal of Australia|March 22, 2012
The need for genetic studies of Indigenous AustraliansGareth S Baynam
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|August 17, 2010
A child with an FGFR3 mutation, a laterality disorder and an hepatoblastoma: novel associations and possible gene-environment interactionsGareth S Baynam, Jack Goldblatt
The Medical Journal of Australia|October 14, 2016
Translating Aboriginal genomics - four letters Closing the GapGareth S Baynam, Glenn Pearson, Jenefer Blackwell
The Medical Journal of Australia|June 23, 2020
Protecting the rare during a rare pandemicGareth S Baynam, Carol Wicking, Kaustuv Bhattacharya, et al.
The Medical Journal of Australia|April 28, 2017
Prevalence of microcephaly in an Australian population-based birth defects register, 1980-2015Michele Hansen, Paul K Armstrong, Carol Bower, et al.
Birth Defects Research|June 9, 2022
The risk of major structural birth defects associated with seasonal influenza vaccination during pregnancy: A population-based cohort studyMohinder Sarna, Gavin F Pereira, Damien Foo, et al.
Journal of Paediatrics and Child Health|May 29, 2021
Birth prevalence of congenital heart defects in Western Australia, 1990-2016Michele Hansen, Kathryn Greenop, Deane Yim, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|July 23, 2013
Objective monitoring of mTOR inhibitor therapy by three-dimensional facial analysisGareth S Baynam, Mark Walters, Hugh Dawkins, et al.
Journal of Paediatrics and Child Health|November 25, 2014
Report and review of described associations of Mayer-Rokitansky-Küster-Hauser syndrome and Silver-Russell syndromeMary B Abraham, Karen Carpenter, Gareth S Baynam, et al.
The Journal of Clinical Endocrinology and Metabolism|September 17, 2013
Overexpression of aromatase associated with loss of heterozygosity of the STK11 gene accounts for prepubertal gynecomastia in boys with Peutz-Jeghers syndromeSeungmin Ham, Sarah J Meachem, Catherine S Choong, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
The Medical Journal of Australia|March 22, 2012
The need for genetic studies of Indigenous AustraliansGareth S Baynam
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|August 17, 2010
A child with an FGFR3 mutation, a laterality disorder and an hepatoblastoma: novel associations and possible gene-environment interactionsGareth S Baynam, Jack Goldblatt
The Medical Journal of Australia|October 14, 2016
Translating Aboriginal genomics - four letters Closing the GapGareth S Baynam, Glenn Pearson, Jenefer Blackwell
The Medical Journal of Australia|June 23, 2020
Protecting the rare during a rare pandemicGareth S Baynam, Carol Wicking, Kaustuv Bhattacharya, et al.
The Medical Journal of Australia|April 28, 2017
Prevalence of microcephaly in an Australian population-based birth defects register, 1980-2015Michele Hansen, Paul K Armstrong, Carol Bower, et al.
Birth Defects Research|June 9, 2022
The risk of major structural birth defects associated with seasonal influenza vaccination during pregnancy: A population-based cohort studyMohinder Sarna, Gavin F Pereira, Damien Foo, et al.
Journal of Paediatrics and Child Health|May 29, 2021
Birth prevalence of congenital heart defects in Western Australia, 1990-2016Michele Hansen, Kathryn Greenop, Deane Yim, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|July 23, 2013
Objective monitoring of mTOR inhibitor therapy by three-dimensional facial analysisGareth S Baynam, Mark Walters, Hugh Dawkins, et al.
Journal of Paediatrics and Child Health|November 25, 2014
Report and review of described associations of Mayer-Rokitansky-Küster-Hauser syndrome and Silver-Russell syndromeMary B Abraham, Karen Carpenter, Gareth S Baynam, et al.
The Journal of Clinical Endocrinology and Metabolism|September 17, 2013
Overexpression of aromatase associated with loss of heterozygosity of the STK11 gene accounts for prepubertal gynecomastia in boys with Peutz-Jeghers syndromeSeungmin Ham, Sarah J Meachem, Catherine S Choong, et al.
Pageof 2