G. Cross

发表

Large-scale discovery of novel genetic causes of developmental disorders

Tomas W. Fitzgerald, M. Hurles, J. Barrett, 2014, Nature.

Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

G. J. Swaminathan, N. Carter, M. Hurles, 2019, American journal of human genetics.

A neuropsychological-genetic profile of atypical cri du chat syndrome: implications for prognosis

A. Green, L. Willatt, K. Cornish, 1999, Journal of medical genetics.

Association of the dopamine transporter (DAT1) 10/10-repeat genotype with ADHD symptoms and response inhibition in a general population sample

J. Swanson, C. Hollis, D. Morisano, 2005, Molecular Psychiatry.

Are Medullary Breast Cancers an Indication for BRCA1 Mutation Screening? A Mutation Analysis of 42 Cases of Medullary Breast Cancer

I. Ellis, S. Pinder, R. Blamey, 2004, Breast Cancer Research and Treatment.

Loss of Heterozygosity in Bilateral Breast Cancer

I. Ellis, R. Blamey, S. Pinder, 2000, Breast Cancer Research and Treatment.

Differential Impact of the FMR-1 Full Mutation on Memory and Attention Functioning: A Neuropsychological Perspective

F. Munir, K. Cornish, G. Cross, 2001, Journal of Cognitive Neuroscience.

Spatial Cognition in Males With Fragile-X Syndrome: Evidence for a Neuropsychological Phenotype

F. Munir, K. Cornish, G. Cross, 1999, Cortex.

The nature of the spatial deficit in young females with Fragile-X syndrome: a neuropsychological and molecular perspective

F. Munir, K. Cornish, G. Cross, 1998, Neuropsychologia.

BRCA1 c.2845insA is a recurring mutation with a founder effect in Singapore Malay women with early onset breast/ovarian cancer

J. Sng, G. Cross, Azhar Ali, 2003, Journal of medical genetics.

Immunostaining in the context of loss mismatch repair function: interpretive confounders and cautionary tales!

M. Ilyas, P. Kaye, G. Cross, 2012, Histopathology.

Cystic fibrosis mutation analysis: Report from 22 U.K. regional genetics laboratories

M. Tassabehji, D. Barton, G. Taylor, 1995, Human mutation.