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Journal of Paediatrics and Child Health|April 23, 2013
Update on the investigation of children with delayed developmentNatalie Silove, Felicity Collins, Carolyn EllawayAmerican Journal of Medical Genetics. Part A|June 10, 2017
Growth charts for Australian children with achondroplasiaLouise Tofts, Sandeep Das, Felicity Collins, et al.Prenatal Diagnosis|July 18, 2003
Three different origins for apparent triploid/diploid mosaicsArt Daniel, Zhanhe Wu, Artur Darmanian, et al.European Journal of Human Genetics : EJHG|January 20, 2022
A systematic review of geographical inequities for accessing clinical genomic and genetic services for non-cancer related rare diseaseStephanie Best, Nada Vidic, Kim An, et al.Journal of Paediatrics and Child Health|October 8, 2014
Joint hypermobility syndrome: a review for cliniciansVerity Pacey, Louise Tofts, Alison Wesley, et al.American Journal of Medical Genetics. Part A|February 28, 2022
The prevalence and impact of orthostatic intolerance in young women across the hypermobility spectrumKaren C Peebles, Isabella Tan, Mark Butlin, et al.Journal of the American Society of Nephrology : JASN|July 29, 2005
Multicystic dysplastic kidney and variable phenotype in a family with a novel deletion mutation of PAX2Jeffery Fletcher, Min Hu, Yemima Berman, et al.Cancer Research|February 28, 2007
Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesisElizabeth M Algar, Luke St Heaps, Artur Darmanian, et al.Clinical Dysmorphology|December 1, 2005
Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual associationKatherine Neas, Greg Peters, Julianne Jackson, et al.European Journal of Human Genetics : EJHG|November 26, 2024
Assessing the unmet needs of genomic testing in Australia: a geospatial explorationSarah Casauria, Felicity Collins, Susan M White, et al.Pageof 4