G. Turner

发表

Increasing evidence that germline mutations in CHEK2 do not cause Li‐Fraumeni syndrome

R. Eeles, R. Houlston, M. Yuille, 2002, Human mutation.

Linkage analysis of early-onset breast and ovarian cancer families, with markers on the long arm of chromosome 17.

D. Kelsell, D. Bishop, N. Spurr, 1993, American journal of human genetics.

Identification of the familial cylindromatosis tumour-suppressor gene

A. Ashworth, S. Seal, M. Stratton, 2000, Nature Genetics.

Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12–q13

S. Seal, M. Stratton, R. Siebert, 2000, Human Genetics.

Heterogeneity in Li-Fraumeni families: p53 mutation analysis and immunohistochemical staining.

L. Bobrow, D. Barnes, C. MacGeoch, 1995, Journal of medical genetics.

Genetic susceptibility to colorectal cancer in patients under 45 years of age

D. Bishop, B. Ward, D. Bishop, 1994, The British journal of surgery.

An unusual solitary lesion on the glans penis

C. Blick, A. Muneer, I. Ali, 2009, Clinical and experimental dermatology.

A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34.

C. Woods, G. Turner, G. Karbani, 2000, American journal of human genetics.