K. Harrop

Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia.

S. Mundlos, F. Westermann, N. Laing, 2001 .

22q11 deletions in patients with conotruncal heart defects

C. Bower, K. Harrop, I. Walpole, 1998, Journal of paediatrics and child health.

Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia

S. Mundlos, F. Westermann, N. Laing, 2001, Nature Genetics.

Evaluating Genetic Counseling: Client Expectations, Psychological Adjustment and Satisfaction with Service

J. Goldblatt, P. O'Leary, K. Harrop, 2005, Journal of Genetic Counseling.

Genetic testing for Alzheimer's disease

P. Panegyres, K. Harrop, J. Goldblatt, 2000, The Medical journal of Australia.

Diabetes in India : The Current Scenario INTERVIEW Clinical Perspectives on Diabetic Retinopathy

K. Harrop, T. Glauser, B. M. Hegde, 2010 .

Study protocol of a multicentre cohort pilot study implementing an expanded preconception carrier-screening programme in metropolitan and regional Western Australia

J. Beilby, G. Ravenscroft, N. Laing, 2019, BMJ Open.

Genetic testing for Alzheimer's disease

P. Panegyres, K. Harrop, J. Goldblatt, 2000, The Medical journal of Australia.