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Robin Forbes

Showing results (1-10 of 27) with videos related to

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Journal of Paediatrics and Child Health|May 30, 2020
Communication about spinal muscular atrophy and genetic risk within families: An Australian pilot studyEllen Pieper, Adrienne Sexton, Monique M Ryan, et al.
Brain Research|November 19, 2013
Neonatal RU-486 (mifepristone) exposure increases androgen receptor immunoreactivity and sexual behavior in male ratsRobin Forbes-Lorman, Anthony P Auger, Catherine J Auger
American Journal of Medical Genetics. Part A|August 13, 2008
Consumer contribution to the delivery of genetic health servicesAmy Nisselle, Robin Forbes, Agnes Bankier, et al.
Journal of Paediatrics and Child Health|October 11, 2007
Community-wide screening for cystic fibrosis carriers could replace newborn screening for the diagnosis of cystic fibrosisJohn Massie, Robin Forbes, Desiree Dusart, et al.
Journal of Child Neurology|December 21, 2019
False Negative Carrier Screening in Spinal Muscular AtrophySophie Butcher, Melanie Smith, Ian R Woodcock, et al.
BMC Health Services Research|November 11, 2025
Quality improvement project to transition psychosocial oncology clinical care to a telehealth workflow during the COVID-19 pandemic: a quasi-experimental studyRickinder Sethi, Brendan Lyver, Jaswanth Gorla, et al.
Journal of Genetic Counseling|October 19, 2007
Letter to the editor journal of genetic counseling. When you care enough to do your very best: genetic counselor experiences of compassion fatigueMargaret Sahhar, Michael Bogwitz, Erica Brown, et al.
American Journal of Medical Genetics. Part A|August 17, 2013
5q31.3 Microdeletion syndrome: clinical and molecular characterization of two further casesNatasha Brown, Trent Burgess, Robin Forbes, et al.
Journal of Paediatrics and Child Health|October 7, 2015
'A short time but a lovely little short time': Bereaved parents' experiences of having a child with spinal muscular atrophy type 1Emily J Higgs, Belinda J McClaren, Margaret Ar Sahhar, et al.
Journal of Child Neurology|September 24, 2014
X-linked Recessive Distal Myopathy With Hypertrophic Cardiomyopathy Caused by a Novel Mutation in the FHL1 GeneColleen D'Arcy, Voula Kanellakis, Robin Forbes, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Journal of Paediatrics and Child Health|May 30, 2020
Communication about spinal muscular atrophy and genetic risk within families: An Australian pilot studyEllen Pieper, Adrienne Sexton, Monique M Ryan, et al.
Brain Research|November 19, 2013
Neonatal RU-486 (mifepristone) exposure increases androgen receptor immunoreactivity and sexual behavior in male ratsRobin Forbes-Lorman, Anthony P Auger, Catherine J Auger
American Journal of Medical Genetics. Part A|August 13, 2008
Consumer contribution to the delivery of genetic health servicesAmy Nisselle, Robin Forbes, Agnes Bankier, et al.
Journal of Paediatrics and Child Health|October 11, 2007
Community-wide screening for cystic fibrosis carriers could replace newborn screening for the diagnosis of cystic fibrosisJohn Massie, Robin Forbes, Desiree Dusart, et al.
Journal of Child Neurology|December 21, 2019
False Negative Carrier Screening in Spinal Muscular AtrophySophie Butcher, Melanie Smith, Ian R Woodcock, et al.
BMC Health Services Research|November 11, 2025
Quality improvement project to transition psychosocial oncology clinical care to a telehealth workflow during the COVID-19 pandemic: a quasi-experimental studyRickinder Sethi, Brendan Lyver, Jaswanth Gorla, et al.
Journal of Genetic Counseling|October 19, 2007
Letter to the editor journal of genetic counseling. When you care enough to do your very best: genetic counselor experiences of compassion fatigueMargaret Sahhar, Michael Bogwitz, Erica Brown, et al.
American Journal of Medical Genetics. Part A|August 17, 2013
5q31.3 Microdeletion syndrome: clinical and molecular characterization of two further casesNatasha Brown, Trent Burgess, Robin Forbes, et al.
Journal of Paediatrics and Child Health|October 7, 2015
'A short time but a lovely little short time': Bereaved parents' experiences of having a child with spinal muscular atrophy type 1Emily J Higgs, Belinda J McClaren, Margaret Ar Sahhar, et al.
Journal of Child Neurology|September 24, 2014
X-linked Recessive Distal Myopathy With Hypertrophic Cardiomyopathy Caused by a Novel Mutation in the FHL1 GeneColleen D'Arcy, Voula Kanellakis, Robin Forbes, et al.
Pageof 3