A. Raizis

发表

A novel 5' (4041insA) mutation in a patient with numerous manifestations of Cowden disease.

M. Ferguson, A. Raizis, D. Nicholls, 2000, The Journal of investigative dermatology.

Effect of nonsense mutations on PTEN mRNA stability

P. George, M. Ferguson, A. Raizis, 2000, Human Genetics.

A mitotic recombination in Wilms tumor occurs between the parathyroid hormone locus and 11p13

A. Reeve, D. Becroft, A. Raizis, 2004, Human Genetics.

The characterization of ovine genes for atrial, brain, and C-type natriuretic peptides.

V. Cameron, E. Espiner, P. George, 1999, Domestic animal endocrinology.

Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells

A. Reeve, S. Sih, A. Reeve, 1989, Molecular and cellular biology.

Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren's syndrome.

P. George, C. Atkinson, B. Robinson, 1998, Molecular pathology : MP.

Short report Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren’s syndrome

P. George, B. Robinson, M. Ferguson, 1998 .

Four cases of autosomal dominant hypocalcaemia with hypercalciuria including two with novel mutations in the calcium-sensing receptor gene

S. Soule, C. Florkowski, P. Frengley, 2011, Annals of clinical biochemistry.

A bisulfite method of 5-methylcytosine mapping that minimizes template degradation.

J. Jost, J P Jost, A M Raizis, 1995, Analytical biochemistry.

Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studies.

W. Lam, P. Boutros, T. Corson, 2013, The Lancet. Oncology.

Structural analysis of the human insulin-like growth factor-II P3 promoter.

M. Eccles, A. Reeve, A. Raizis, 1993, The Biochemical journal.

Role of genetic testing in retinoblastoma management at a tertiary referral centre

P. George, A. Vincent, Monika A Pradhan, 2010, Clinical & experimental ophthalmology.

Improved clinical management of retinoblastoma through gene testing.

R. Clemett, P. George, R. Corbett, 2002, The New Zealand medical journal.

DNA hypermethylation/boundary control loss identified in retinoblastomas associated with genetic and epigenetic inactivation of the RB1 gene promoter

B. Gallie, P. George, A. Foucal, 2020, Epigenetics.

Novel inactivating mutation of the calcium‐sensing receptor in a young woman with mild hypercalcaemia

C. Florkowski, L. Que, A. Raizis, 2014, Internal medicine journal.

Expanding the clinical and radiological phenotypes of leukoencephalopathy due to biallelic HMBS mutations

P. Lockhart, M. Bahlo, E. Janus, 2021, American journal of medical genetics. Part A.

Trilateral Retinoblastoma in a Patient With Peutz–Jeghers Syndrome

L. Aaltonen, D. Lohmann, P. George, 2013, American journal of medical genetics. Part A.

Three families with Perry syndrome from distinct parts of the world.

M. Okun, Z. Wszolek, A. Strongosky, 2014, Parkinsonism & related disorders.

A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp)

D. Lambie, C. Florkowski, W. Siu, 2018, Annals of clinical biochemistry.

Spectrum of MECP2 mutations in New Zealand Rett syndrome patients.

P. George, M. Saleem, R. Mackay, 2009, The New Zealand medical journal.