Concepedia

Fiona A. McKenzie

FA

Statistics

Publications

2

Citations

252

H-Index

2

Active since

2013

Affiliations

The University of Sydney(Current)

Children's Hospital at Westmead

Boston Children's Hospital

Translational Research Institute

The University of Queensland

Fiona A. McKenzie is an author at The University of Sydney specializing in molecular genetics, genetics, and human genetics.

Publications per year

2013–2014

2

Publications

2

Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans

Jan Halbritter, Albane A. Bizet, Miriam Schmidts et al. · The American Journal of Human Genetics · 2013 · 231 citations · Full text

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The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type V

Syndia Lazarus, Aideen McInerney‐Leo, Fiona A. McKenzie et al. · BMC Musculoskeletal Disorders · 2014 · 21 citations · Full text

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