An exclusion map covering the whole genome: a new challenge for genetic epidemiologists?

Por Clerget-Darpoux, F, Bonaïti-Pellié, C
Publicado em 1993

An epidemiological and genetic study of congenital profound deafness in Tunisia (governorate of Nabeul).

Por Ben Arab, S, Bonaïti-Pellié, C, Belkahia, A
Publicado em 1990

Excess of cancer deaths in grandparents of patients with retinoblastoma.

Por Bonaïti-Pellié, C, Briard-Guillemot, M L
Publicado em 1980

Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.

Por Moutou, C, Junien, C, Henry, I, Bonaïti-Pellié, C
Publicado em 1992

Conclusions of segregation analysis for family data generated under two-locus models.

Por Dizier, M H, Bonaïti-Pellié, C, Clerget-Darpoux, F
Publicado em 1993

POINTER correctly estimates the transmission probabilities under the general transmission model in the case of incomplete selection.

Por Dizier, M H, Bonaiti-Pellié, C, Clerget-Darpoux, F
Publicado em 1992

HLA-associated diseases: a new method for performing linkage analysis with other markers than HLA.

Por Clerget-Darpoux, F, Babron, M C, Bonaïti-Pellie, C
Publicado em 1984

Hereditary non-polyposis colorectal cancer: current risks of colorectal cancer largely overestimated

Por Carayol, J, Khlat, M, Maccario, J, Bonaiti-Pellie, C
Publicado em 2002

Sex differences in cancer risk among germline p53 mutation carriers

Por Chompret, A, Brugières, L, Bonaïti-Pellié, C, Feunteun, J
Publicado em 2004

An epidemiological and genetic study of facial clefting in France. II Segregation analysis.

Por Demenais, F, Bonaïti-Pellié, C, Briard, M L, Feingold, J
Publicado em 1984

Segregation analysis of Alagille syndrome.

Por Dhorne-Pollet, S, Deleuze, J F, Hadchouel, M, Bonaïti-Pellié, C
Publicado em 1994

Vagal overactivity: a risk factor of sudden infant death syndrome?

Por Shojaei-Brosseau, T, Bonaiti-Pellie, C, Lyonnet, S, Feingold, J, Lucet, V
Publicado em 2003

Linkage of familial breast cancer to chromosome 17q21 may not be restricted to early-onset disease.

Por Margaritte, P, Bonaiti-Pellie, C, King, M C, Clerget-Darpoux, F
Publicado em 1992

Sensitivity and predictive value of criteria for p53 germline mutation screening

Por CHOMPRET, A., ABEL, A., STOPPA-LYONNET, D., BRUGIERES, L., PAGES, S., FEUNTEUN, J., BONAITI-PELLIE, C.
Publicado em 2001

Genetic study of transthyretin amyloid neuropathies: carrier risks among French and Portuguese families

Por Plante-Bordeneuve, V, Carayol, J, Ferreira, A, Adams, D, Clerget-Darpoux, F, Misrahi, M, Said, G, Bonaiti-Pellie, C
Publicado em 2003

The French Wilms' tumour study: no clear evidence for cancer prone families.

Por Moutou, C, Hochez, J, Chompret, A, Tournade, M F, Le Bihan, C, Zucker, J M, Lemerle, J, Bonaïti-Pellié, C
Publicado em 1994

French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion.

Por Lavedan, C, Hofmann-Radvanyi, H, Boileau, C, Bonaïti-Pellié, C, Savoy, D, Shelbourne, P, Duros, C, Rabes, J P, Dehaupas, I, Luce, S
Publicado em 1994

Impact of the MDM2 SNP309 and p53 Arg72Pro polymorphism on age of tumour onset in Li‐Fraumeni syndrome

Por Bougeard, G, Baert‐Desurmont, S, Tournier, I, Vasseur, S, Martin, C, Brugieres, L, Chompret, A, Paillerets, B Bressac‐de, Stoppa‐Lyonnet, D, Bonaiti‐Pellie, C, Frebourg, T
Publicado em 2006

BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group.

Por Stoppa-Lyonnet, D, Laurent-Puig, P, Essioux, L, Pagès, S, Ithier, G, Ligot, L, Fourquet, A, Salmon, R J, Clough, K B, Pouillart, P, Bonaïti-Pellié, C, Thomas, G
Publicado em 1997

P53 germline mutations in childhood cancers and cancer risk for carrier individuals

Por Chompret, A, Brugières, L, Ronsin, M, Gardes, M, Dessarps-Freichey, F, Abel, A, Hua, D, Ligot, L, Dondon, M-G, Paillerets, B Bressac-de, Frébourg, T, Lemerle, J, Bonaïti-Pellié, C, Feunteun, J
Publicado em 2000