J. Peverall

发表

Analysis of early pleural fluid samples in patients with mesothelioma: A case series exploration of morphology, BAP1, and CDKN2A status with implications for the concept of mesothelioma in situ in cytology

Y. C. Lee, J. Creaney, A. Louw, 2022, Cancer cytopathology.

Equivocal ALK fluorescence in‐situ hybridization (FISH) cases may benefit from ancillary ALK FISH probe testing

M. Christie, N. Pavlakis, S. O'toole, 2015, Histopathology.

Histological comparison of partial hydatidiform mole and trisomy gestation specimens.

C. Bharat, M. Crook, C. Stewart, 2016, Pathology.

Detailed molecular cytogenetic characterisation of the myeloid cell line U937 reveals the fate of homologous chromosomes and shows that centromere capture is a feature of genome instability

L. Campbell, M. Wall, J. Peverall, 2020, Molecular cytogenetics.

Genome organization and the role of centromeres in evolution of the erythroleukaemia cell line HEL

L. Campbell, M. Wall, J. Peverall, 2013, Evolution, medicine, and public health.

MDM2/CDK4 gene amplification in large/deep-seated 'lipomas': incidence, predictors and clinical significance.

P. Robbins, R. Carey-Smith, D. Spagnolo, 2016, Pathology.

Further heterogeneity in Silver–Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement

J. Beilby, K. Woodward, Gillian M. Arscott, 2021, American journal of medical genetics. Part A.

Detection of Y‐chromosome in gonadal tumours using fluorescence in situ hybridization: diagnostic value in intersex conditions including older patients with clinically unsuspected androgen insensitivity syndrome

C. Beaton, M. Crook, J. Peverall, 2007, Histopathology.

Structural chromosome disruption of the NR3C2 gene causing pseudohypoaldosteronism type 1 presenting in infancy

T. Jones, T. Ly, B. Lewis, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Severe γ-sarcoglycanopathy caused by a novel missense mutation and a large deletion

N. Laing, R. Johnsen, B. Kakulas, 2000, Neuromuscular Disorders.

Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance

J. Beilby, F. McKenzie, K. Woodward, 2019, Molecular genetics & genomic medicine.

Evaluation of fluorescence in‐situ hybridization in monomorphic endometrial stromal neoplasms and their histological mimics: a review of 49 cases

C. Stewart, A. Murch, Y. Leung, 2014, Histopathology.

A review of structural brain abnormalities in Pallister‐Killian syndrome

J. Beilby, K. Woodward, G. Baynam, 2017, Molecular genetics & genomic medicine.

Large nested melanoma: a clinicopathological, morphometric and cytogenetic study of 12 cases.

B. Wood, C. van Vliet, J. Peverall, 2020, Pathology.

Correlation of FISH and PRAME Immunohistochemistry in Ambiguous Superficial Cutaneous Melanocytic Proliferations

B. Wood, C. van Vliet, J. Peverall, 2021, The American Journal of dermatopathology.

Identification of a novel deletion of the entire OCRL1 gene detected by FISH analysis in a family with Lowe syndrome

J. Goldblatt, E. Edkins, A. Murch, 2000, Clinical genetics.

The utility of MDM2 and CDK4 immunohistochemistry in the diagnosis of lipomatous tumours and correlation with fluorescence in situ hybridisation

M. Platten, B. Amanuel, B. Dessauvagie, 2012 .