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Page 1
Genetic testing for Alzheimer's disease.
Panegyres PK, Goldblatt J, Walpole I, Connor C, Liebeck T, Harrop K. Panegyres PK, et al. Among authors: harrop k. Med J Aust. 2000 Apr 3;172(7):339-43. doi: 10.5694/j.1326-5377.2000.tb123984.x. Med J Aust. 2000. PMID: 10844923
22q11 deletions in patients with conotruncal heart defects.
Worthington S, Bower C, Harrop K, Loh J, Walpole I. Worthington S, et al. Among authors: harrop k. J Paediatr Child Health. 1998 Oct;34(5):438-43. doi: 10.1046/j.1440-1754.1998.00262.x. J Paediatr Child Health. 1998. PMID: 9767506
Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia.
Nürnberg P, Thiele H, Chandler D, Höhne W, Cunningham ML, Ritter H, Leschik G, Uhlmann K, Mischung C, Harrop K, Goldblatt J, Borochowitz ZU, Kotzot D, Westermann F, Mundlos S, Braun HS, Laing N, Tinschert S. Nürnberg P, et al. Among authors: harrop k. Nat Genet. 2001 May;28(1):37-41. doi: 10.1038/ng0501-37. Nat Genet. 2001. PMID: 11326272
Foreword - Why specialist lenses?
Harrop K, Beerten R, Steenbekkers G, Voltz K, Johnson L, Siergey J. Harrop K, et al. Cont Lens Anterior Eye. 2023 Feb;46(1):101797. doi: 10.1016/j.clae.2022.101797. Epub 2022 Dec 23. Cont Lens Anterior Eye. 2023. PMID: 36566122 No abstract available.
13 results