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Linda Baskcomb

The Royal Marsden NHS Foundation Trust

10

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592

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Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor

2008 Nature Genetics
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Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation

2007 Journal of Medical Genetics
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SHORT REPORT Evaluation of RAD50 in familial breast cancer predisposition

2006
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A Genome wide linkage search for breast cancer susceptibility genes

2006 Centre for Health Research; Faculty of Health; Institute of Health and Biomedical Innovation
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PHOX2B analysis in non-syndromic neuroblastoma cases shows novel mutations and genotype-phenotype associations

2006 American Journal of Medical Genetics Part A
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A genome wide linkage search for breast cancer susceptibility genes.

2006 Genes, Chromosomes and Cancer
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Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour

2005 Journal of Medical Genetics
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Citations (100)