Author

RJ McKinlay Gardner

Institution: University of Otago

Observed institutions: The Royal Melbourne Hospital, Royal Children's Hospital, The University of Melbourne, Murdoch Children's Research Institute, University of Otago

OpenAlex ID: A5111991176

High frequency hearing loss correlated with mutations in the GJB2 gene

2000 · Stephen A Wilcox, Kerryn Saunders, et al. · Human Genetics · 201

Deletions Revealing Recessive Genes: Deletions that reveal recessive genes

2007 · David J Coman, RJ McKinlay Gardner · European Journal of Human Genetics · 93

Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome

2005 · Birgitt Schüle, Mohammed Albalwi, et al. · BMC Medical Genetics · 71

TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families

2011 · Elena Andreucci, Salim Aftimos, et al. · Orphanet Journal of Rare Diseases · 62

Frequency of the ATM IVS10-6T→G variant in Australian multiple-case breast cancer families

2004 · Geoffrey J Lindeman, Melody Hiew, et al. · Breast Cancer Research · 16

Gardner and Sutherland's Chromosome Abnormalities and Genetic Counseling

2025 · David J. Amor, RJ McKinlay Gardner · 2

Works count: 6

Citation count: 445

H-index: 5

I10-index: 5