D. Forman, R. T. Oliver, A. R. Brett, S. G. Marsh, J. H. Moses et al., Familial testicular cancer: a report of the UK family register, estimation of risk and an HLA class 1 sib-pair analysis, British Journal of Cancer, vol.65, issue.2, pp.255-262, 1992.
DOI : 10.1038/bjc.1992.51

K. Heimdal, H. Olsson, S. Tretli, P. Flodgren, A. L. Borresen et al., Familial testicular cancer in Norway and southern Sweden, British Journal of Cancer, vol.73, issue.7, pp.964-969, 1996.
DOI : 10.1038/bjc.1996.173

K. Hemminki and X. Li, Familial risk in testicular cancer as a clue to a heritable and environmental aetiology, British Journal of Cancer, vol.66, issue.9, pp.1765-1770, 2004.
DOI : 10.1038/sj.bjc.6601714

C. Dong and K. Hemminki, Modification of cancer risks in offspring by sibling and parental cancers from 2,112,616 nuclear families, International Journal of Cancer, vol.355, issue.1, pp.144-150, 2001.
DOI : 10.1002/1097-0215(200102)9999:9999<::AID-IJC1147>3.0.CO;2-C

K. Heimdal, H. Olsson, S. Tretli, S. D. Fossa, A. L. Borresen et al., A segregation analysis of testicular cancer based on Norwegian and Swedish families, British Journal of Cancer, vol.75, issue.7, pp.1084-1087, 1997.
DOI : 10.1038/bjc.1997.185

P. W. Nicholson and S. J. Harland, Inheritance and testicular cancer, British Journal of Cancer, vol.71, issue.2, pp.421-426, 1995.
DOI : 10.1038/bjc.1995.86

E. A. Rapley, G. P. Crockford, D. Teare, P. Biggs, S. Seal et al., Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours, Nature Genetics, vol.7, issue.2, pp.197-200, 2000.
DOI : 10.1038/72877

E. A. Rapley, G. P. Crockford, D. F. Easton, M. R. Stratton, and D. T. Bishop, Localisation of susceptibility genes for familial testicular germ cell tumour, APMIS, vol.75, issue.1, pp.128-133, 2003.
DOI : 10.1038/ng1195-241

M. G. Leahy, S. Tonks, J. H. Moses, A. R. Brett, R. Huddart et al., Candidate regions for a testicular cancer susceptibility gene, Human Molecular Genetics, vol.4, issue.9, pp.1551-1555, 1995.
DOI : 10.1093/hmg/4.9.1551
URL : http://hmg.oxfordjournals.org/cgi/content/short/4/9/1551

E. A. Rapley, G. P. Crockford, D. F. Easton, M. Stratton, and D. T. Bishop, The Genetics of Testicular Germ Cell Tumours, Germ Cell Tumours, pp.1-22, 2002.
DOI : 10.1007/978-1-4471-3281-3_1

A. Ganguly, M. J. Rock, and D. J. Prockop, Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes., Proceedings of the National Academy of Sciences, vol.90, issue.21, pp.10325-10329, 1993.
DOI : 10.1073/pnas.90.21.10325

H. O. Adami, R. Bergstrom, M. Mohner, W. Zatonski, H. Storm et al., Testicular cancer in nine northern european countries, International Journal of Cancer, vol.336, issue.1, pp.33-38, 1994.
DOI : 10.1002/ijc.2910590108

R. Bergstrom, H. O. Adami, M. Mohner, W. Zatonski, H. Storm et al., Increase in Testicular Cancer Incidence in Six European Countries: a Birth Cohort Phenomenon, JNCI Journal of the National Cancer Institute, vol.88, issue.11, pp.727-733, 1996.
DOI : 10.1093/jnci/88.11.727

L. M. Brown, L. M. Pottern, R. N. Hoover, S. S. Devesa, P. Aselton et al., Testicular Cancer in the United States: Trends in Incidence and Mortality, International Journal of Epidemiology, vol.15, issue.2, pp.164-170, 1986.
DOI : 10.1093/ije/15.2.164

J. M. Davies, TESTICULAR CANCER IN ENGLAND AND WALES: SOME EPIDEMIOLOGICAL ASPECTS, The Lancet, vol.317, issue.8226, pp.928-932, 1981.
DOI : 10.1016/S0140-6736(81)91625-1

G. R. Abecasis, S. S. Cherny, W. O. Cookson, C. , and L. R. , Merlin???rapid analysis of dense genetic maps using sparse gene flow trees, Nature Genetics, vol.30, issue.1, pp.97-101, 2002.
DOI : 10.1038/ng786

M. S. Mcpeek and L. Sun, Statistical Tests for Detection of Misspecified Relationships by Use of Genome-Screen Data, The American Journal of Human Genetics, vol.66, issue.3, pp.1076-1094, 2000.
DOI : 10.1086/302800

G. R. Abecasis, S. S. Cherny, W. O. Cookson, C. , and L. R. , GRR: graphical representation of relationship errors, Bioinformatics, vol.17, issue.8, pp.742-743, 2001.
DOI : 10.1093/bioinformatics/17.8.742
URL : http://bioinformatics.oxfordjournals.org/cgi/content/short/17/8/742

D. F. Gudbjartsson, K. Jonasson, M. L. Frigge, and A. Kong, Allegro, a new computer program for multipoint linkage analysis, Nature Genetics, vol.44, issue.1, pp.12-13, 2000.
DOI : 10.1002/(SICI)1098-2272(1999)16:3<225::AID-GEPI1>3.0.CO;2-#

A. Kong and N. J. Cox, Allele-Sharing Models: LOD Scores and Accurate Linkage Tests, The American Journal of Human Genetics, vol.61, issue.5, pp.1179-1188, 1997.
DOI : 10.1086/301592
URL : http://doi.org/10.1086/301592

K. W. Broman, J. C. Murray, V. C. Sheffield, R. L. White, W. et al., Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in Recombination, The American Journal of Human Genetics, vol.63, issue.3, pp.861-869, 1998.
DOI : 10.1086/302011

L. Kruglyak, M. J. Daly, M. P. Reeve-daly, and E. S. Lander, Parametric and nonparametric linkage analysis: a unified multipoint approach, Am.J.Hum.Genet, vol.58, pp.1347-1363, 1996.

N. Risch, Linkage strategies for genetically complex traits. I. Multilocus models, Am. J. Hum. Genet, vol.46, pp.222-228, 1990.

J. Ott, Computer-simulation methods in human linkage analysis., Proceedings of the National Academy of Sciences, vol.86, issue.11, pp.4175-4178, 1989.
DOI : 10.1073/pnas.86.11.4175
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC287412

D. Weeks, J. Ott, and G. M. Lathrop, SLINK: a general simulation program for linkage analysis, Am.J.Hum.Genet, vol.47, p.204, 1990.