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Georgina Hollway

Showing results (1-10 of 13) with videos related to

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Birth Defects Research. Part C, Embryo Today : Reviews|September 28, 2005
Vertebrate myotome developmentGeorgina Hollway, Peter Currie
The Medical Journal of Australia|March 23, 2023
The Queensland IMplementation of PRecision Oncology in brEast cancer (Q-IMPROvE) pilot studyAmy E McCart Reed, Georgina Hollway, , et al.
Pharmacogenomics|March 5, 2021
Developing a gene panel for pharmacoresistant epilepsy: a review of epilepsy pharmacogeneticsAstrid J Rodriguez-Acevedo, Louisa G Gordon, Nicola Waddell, et al.
Epilepsia|September 9, 2022
Early cost-utility analysis of genetically guided therapy for patients with drug-resistant epilepsyLouisa G Gordon, Thomas M Elliott, Carmen Bennett, et al.
European Journal of Human Genetics : EJHG|March 2, 2023
Evaluation and pilot testing of a multidisciplinary model of care to mainstream genomic testing for paediatric inborn errors of immunityTatiane Yanes, Anna Sullivan, Pasquale Barbaro, et al.
Developmental Medicine and Child Neurology|February 22, 2025
Pathogenic variants in chromatin-related genes: Linking immune dysregulation to neuroregression and acute neuropsychiatric disordersRussell C Dale, Shekeeb Mohammad, Velda X Han, et al.
BMC Cancer|May 26, 2026
Whole genome sequencing in oesophageal adenocarcinoma unmasks potential precision therapiesSowmya Sharma, Ho Yi Wong, Rebecca L Johnston, et al.
American Journal of Human Genetics|May 9, 2003
Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardationVera M Kalscheuer, Jiong Tao, Andrew Donnelly, et al.
European Journal of Human Genetics : EJHG|January 13, 2021
Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencingAmali C Mallawaarachchi, Ben Lundie, Yvonne Hort, et al.
Ebiomedicine|March 9, 2026
Integrating breast tumour homologous recombination deficiency status to aid germline BRCA1 and BRCA2 variant classificationCristina Fortuno, Jia Zhang, Lambros T Koufariotis, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Birth Defects Research. Part C, Embryo Today : Reviews|September 28, 2005
Vertebrate myotome developmentGeorgina Hollway, Peter Currie
The Medical Journal of Australia|March 23, 2023
The Queensland IMplementation of PRecision Oncology in brEast cancer (Q-IMPROvE) pilot studyAmy E McCart Reed, Georgina Hollway, , et al.
Pharmacogenomics|March 5, 2021
Developing a gene panel for pharmacoresistant epilepsy: a review of epilepsy pharmacogeneticsAstrid J Rodriguez-Acevedo, Louisa G Gordon, Nicola Waddell, et al.
Epilepsia|September 9, 2022
Early cost-utility analysis of genetically guided therapy for patients with drug-resistant epilepsyLouisa G Gordon, Thomas M Elliott, Carmen Bennett, et al.
European Journal of Human Genetics : EJHG|March 2, 2023
Evaluation and pilot testing of a multidisciplinary model of care to mainstream genomic testing for paediatric inborn errors of immunityTatiane Yanes, Anna Sullivan, Pasquale Barbaro, et al.
Developmental Medicine and Child Neurology|February 22, 2025
Pathogenic variants in chromatin-related genes: Linking immune dysregulation to neuroregression and acute neuropsychiatric disordersRussell C Dale, Shekeeb Mohammad, Velda X Han, et al.
BMC Cancer|May 26, 2026
Whole genome sequencing in oesophageal adenocarcinoma unmasks potential precision therapiesSowmya Sharma, Ho Yi Wong, Rebecca L Johnston, et al.
American Journal of Human Genetics|May 9, 2003
Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardationVera M Kalscheuer, Jiong Tao, Andrew Donnelly, et al.
European Journal of Human Genetics : EJHG|January 13, 2021
Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencingAmali C Mallawaarachchi, Ben Lundie, Yvonne Hort, et al.
Ebiomedicine|March 9, 2026
Integrating breast tumour homologous recombination deficiency status to aid germline BRCA1 and BRCA2 variant classificationCristina Fortuno, Jia Zhang, Lambros T Koufariotis, et al.
Pageof 2