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Familial Cancer|October 11, 2016
Genetically diagnosed Birt-Hogg-Dubé syndrome and familial cerebral cavernous malformations in the same individual: a case reportJames Whitworth, Brian Stausbøl-Grøn, Anne-Bine Skytte
Familial Cancer|November 23, 2016
Truncation of the MSH2 C-terminal 60 amino acids disrupts effective DNA mismatch repair and is causative for Lynch syndromeEva Wielders, Elly Delzenne-Goette, Rob Dekker, et al.
Familial Cancer|November 30, 2016
Four generations of SDHB-related disease: complexities in managementU Srirangalingam, M LeCain, N Tufton, et al.
Familial Cancer|November 21, 2016
The hereditary nature of small cell carcinoma of the ovary, hypercalcemic type: two new familial casesLeora Witkowski, Nancy Donini, Rebecca Byler-Dann, et al.
Familial Cancer|February 1, 2008
Muir-Torre Syndrome: expanding the genotype and phenotype--a further family with a MSH6 mutationH R Murphy, R Armstrong, D Cairns, et al.
Familial Cancer|February 20, 2008
Tumor histology helps to identify Lynch syndrome among colorectal cancer patientsBrindusa Truta, Yunn-Yi Chen, Amie M Blanco, et al.
Familial Cancer|February 11, 2014
Capsule endoscopy versus magnetic resonance enterography for the detection of small bowel polyps in Peutz-Jeghers syndromeP Urquhart, F Grimpen, G J Lim, et al.
Familial Cancer|March 11, 2014
Duplex value of caveolin-1 in non-small cell lung cancer: a meta analysisDali Chen, Cheng Shen, Heng Du, et al.
Familial Cancer|March 11, 2014
Mosaic partial deletion of the PTEN gene in a patient with Cowden syndromeErin E Salo-Mullen, Jinru Shia, Isaac Brownell, et al.
Familial Cancer|February 9, 2017
Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relativesJessica Ezzell Hunter, Kathleen A Arnold, Jennifer E Cook, et al.
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