Joanne W. Dixon
Christchurch, CAN, New Zealand
Last Updated: 09/26/2026
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Found 10 publications
Correction: Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711.
Journal: European journal of human genetics : EJHG
Published: December 01, 2023
Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711.
Journal: European journal of human genetics : EJHG
Published: August 03, 2021
Constraint and conservation of paired-type homeodomains predicts the clinical outcome of missense variants of uncertain significance.
Journal: Human mutation
Published: October 30, 2019
Successful pregnancies and reduced treatment requirement while breast feeding in a patient with congenital hypoparathyroidism due to homozygous c.68C>A null parathyroid hormone gene mutation.
Journal: BMJ case reports
Published: May 28, 2018
A retrospective audit of the characteristics and treatment outcomes in patients with diabetes-related charcot neuropathic osteoarthropathy.
Journal: The New Zealand medical journal
Published: December 15, 2017
Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis.
Journal: American journal of human genetics
Published: March 30, 2016
Venous thromboembolism rates in patients undergoing major hip and knee joint surgery at Waitemata District Health Board: a retrospective audit.
Journal: Internal medicine journal
Published: September 14, 2014
Mutations in NOTCH1 cause Adams-Oliver syndrome.
Journal: American journal of human genetics
Published: July 02, 2014
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: October 16, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026