S. Antonarakis, . The-nomenclature-working, and . Group, Recommendations for a nomenclature system for human gene mutations, Human Mutation, vol.8, issue.1, pp.1-3, 1998.
DOI : 10.1002/(SICI)1098-1004(1998)11:1<1::AID-HUMU1>3.0.CO;2-O

C. Béroud and T. Soussi, APC gene: database of germline and somatic mutations in human tumors and cell lines, Nucleic Acids Research, vol.24, issue.1, pp.121-124, 1996.
DOI : 10.1093/nar/24.1.121

C. Béroud and T. Soussi, p53 and APC gene mutations: software and databases, Nucleic Acids Research, vol.25, issue.1, p.138, 1997.
DOI : 10.1093/nar/25.1.138

C. Béroud and T. Soussi, p53 gene mutation: software and database, Nucleic Acids Research, vol.26, issue.1, pp.200-204, 1998.
DOI : 10.1093/nar/26.1.200

C. Béroud, F. Verdier, and T. Soussi, p53 gene mutation: software and database, Nucleic Acids Research, vol.24, issue.1, pp.147-150, 1996.
DOI : 10.1093/nar/24.1.147

C. Béroud, D. Joly, C. Gallou, F. Staroz, M. Orfanelli et al., Software and database for the analysis of mutations in the VHL gene, Nucleic Acids Research, vol.26, issue.1, pp.256-258, 1998.
DOI : 10.1093/nar/26.1.256

N. Cariello, L. Cui, C. Béroud, and T. Soussi, Database and software for the analysis of mutations in the human p53 gene, Cancer Res, vol.54, pp.4454-4460, 1994.

G. Collod, C. Béroud, T. Soussi, C. Junien, and C. Boileau, Software and database for the analysis of mutations in the human FBN1 gene, Nucleic Acids Research, vol.24, issue.1, pp.137-140, 1996.
DOI : 10.1093/nar/24.1.137

URL : https://hal.archives-ouvertes.fr/inserm-00143165

G. Collod-béroud, C. Béroud, L. Ades, C. Black, M. Boxer et al., Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene, Nucleic Acids Research, vol.25, issue.1, pp.147-150, 1997.
DOI : 10.1093/nar/25.1.147

G. Collod-béroud, C. Béroud, L. Ades, C. Black, M. Boxer et al., Marfan Database (third edition): new mutations and new routines for the software, Nucleic Acids Research, vol.26, issue.1, pp.229-223, 1998.
DOI : 10.1093/nar/26.1.229

D. Cooper, E. Ball, and M. Krawczak, The human gene mutation database, Nucleic Acids Research, vol.26, issue.1, pp.285-287, 1998.
DOI : 10.1093/nar/26.1.285

R. Cotton, V. Mckusick, and C. Scriver, The HUGO Mutation Database Initiative, Science, vol.279, issue.5347, pp.10-11, 1998.
DOI : 10.1126/science.279.5347.10c

J. Den-dunnen and S. Antonarakis, Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion, Human Mutation, vol.10, issue.1, pp.7-12, 2000.
DOI : 10.1038/ng0795-259

P. Edery, S. Lyonnet, L. Mulligan, A. Pelet, E. Dow et al., Mutations of the RET proto-oncogene in Hirschsprung's disease, Nature, vol.367, issue.6461, pp.378-380, 1994.
DOI : 10.1038/367378a0

C. Gallou, D. Joly, A. Méjean, F. Starosz, N. Martin et al., Mutations of the VHL gene in sporadic renal cell carcinoma: Definition of a risk factor for VHL patients to develop an RCC, Human Mutation, vol.8, issue.6, pp.464-475, 1999.
DOI : 10.1002/(SICI)1098-1004(1996)8:4<348::AID-HUMU8>3.0.CO;2-3

R. Hofstra, R. Landsvater, I. Ceccherini, R. Stulp, T. Stelwagen et al., A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma, Nature, vol.367, issue.6461, pp.375-376, 1994.
DOI : 10.1038/367375a0

C. Jeanpierre, C. Béroud, P. Niaudet, and C. Junien, Software and database for the analysis of mutations in the human WT1 gene, Nucleic Acids Research, vol.26, issue.1, pp.271-274, 1998.
DOI : 10.1093/nar/26.1.271

M. Krawczak, E. Ball, I. Fenton, P. Stenson, S. Abeysinghe et al., Human Gene Mutation Database?A biomedical information and research resource, Human Mutation, vol.90, issue.1, pp.45-51, 2000.
DOI : 10.1007/BF00210743

P. Laurent-puig, C. Béroud, and T. Soussi, APC gene: database of germline and somatic mutations in human tumors and cell lines, Nucleic Acids Research, vol.26, issue.1, pp.269-270, 1998.
DOI : 10.1093/nar/26.1.269

L. Mulligan, J. Kwok, C. Healey, M. Elsdon, C. Eng et al., Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A, Nature, vol.363, issue.6428, pp.458-460, 1993.
DOI : 10.1038/363458a0

S. Olschwang, A. Tiret, P. Laurentpuig, M. Muleris, R. Parc et al., Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients, Cell, vol.75, issue.5, pp.959-968, 1993.
DOI : 10.1016/0092-8674(93)90539-3

G. Romeo, P. Ronchetto, Y. Luo, V. Barone, M. Seri et al., Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease, Nature, vol.367, issue.6461, pp.377-378, 1994.
DOI : 10.1038/367377a0

T. Soussi, K. Dehouche, and C. Béroud, p53 Website and analysis of p53 gene mutations in human cancer: Forging a link between epidemiology and carcinogenesis, Human Mutation, vol.372, issue.1, pp.105-113, 2000.
DOI : 10.1038/372773a0

L. Spirio, S. Olschwang, J. Groden, M. Robertson, W. Samowitz et al., Alleles of the APC gene: An attenuated form of familial polyposis, Cell, vol.75, issue.5, pp.951-957, 1993.
DOI : 10.1016/0092-8674(93)90538-2

M. Varret, J. Rabes, G. Collod-béroud, C. Junien, C. Boileau et al., Software and database for the analysis of mutations in the human LDL receptor gene, Nucleic Acids Research, vol.25, issue.1, pp.172-180, 1997.
DOI : 10.1093/nar/25.1.172

URL : https://hal.archives-ouvertes.fr/inserm-00143593

M. Varret, J. Rabes, R. Thiart, M. Kotze, H. Baron et al., LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis, Nucleic Acids Research, vol.26, issue.1, pp.248-252, 1998.
DOI : 10.1093/nar/26.1.248

F. Xue, H. Yu, L. Maurer, V. Memoli, N. Nutile-mcmenemey et al., Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests, Human Molecular Genetics, vol.3, issue.4, pp.635-638, 1994.
DOI : 10.1093/hmg/3.4.635