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102 results
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Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes.
Boileau C, Jondeau G, Babron MC, Coulon M, Alexandre JA, Sakai L, Melki J, Delorme G, Dubourg O, Bonaïti-Pellié C, et al. Boileau C, et al. Among authors: babron mc. Am J Hum Genet. 1993 Jul;53(1):46-54. Am J Hum Genet. 1993. PMID: 8317497 Free PMC article.
Impact of the diagnosis definition on linkage detection.
Dizier MH, Génin E, Babron MC, Bourgain C. Dizier MH, et al. Among authors: babron mc. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S140. doi: 10.1186/1471-2156-6-S1-S140. BMC Genet. 2005. PMID: 16451600 Free PMC article.
Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex.
Bickeböller H, Campion D, Brice A, Amouyel P, Hannequin D, Didierjean O, Penet C, Martin C, Pérez-Tur J, Michon A, Dubois B, Ledoze F, Thomas-Anterion C, Pasquier F, Puel M, Demonet JF, Moreaud O, Babron MC, Meulien D, Guez D, Chartier-Harlin MC, Frebourg T, Agid Y, Martinez M, Clerget-Darpoux F. Bickeböller H, et al. Among authors: babron mc. Am J Hum Genet. 1997 Feb;60(2):439-46. Am J Hum Genet. 1997. PMID: 9012418 Free PMC article.
Genetics of celiac disease.
Clot F, Babron MC. Clot F, et al. Among authors: babron mc. Mol Genet Metab. 2000 Sep-Oct;71(1-2):76-80. doi: 10.1006/mgme.2000.3045. Mol Genet Metab. 2000. PMID: 11001799 Review.
Strategies for detecting susceptibility genes in a complex disease.
Babron MC, Barillot E, Margaritte-Jeannin P, Clerget-Darpoux F. Babron MC, et al. Genet Epidemiol. 1999;17 Suppl 1:S479-83. doi: 10.1002/gepi.1370170777. Genet Epidemiol. 1999. PMID: 10597479
A systematic study of oligodendrocyte growth factors as candidates for genetic susceptibility to MS. French Multiple Sclerosis Genetics Group.
Mertens C, Brassat D, Reboul J, Eichenbaum-Voline S, Vuillemin-Azais C, Cournu I, Babron MC, Semana G, Edan G, Clanet M, Clerget-Darpoux F, Baron-Van Evercooren A, Lyon-Caen O, Liblau R, Fontaine B. Mertens C, et al. Among authors: babron mc. Neurology. 1998 Sep;51(3):748-53. doi: 10.1212/wnl.51.3.748. Neurology. 1998. PMID: 9748021
Interactive effect of two candidate genes in a disease: extension of the marker-association-segregation chi(2) method.
Dizier MH, Babron MC, Clerget-Darpoux F. Dizier MH, et al. Among authors: babron mc. Am J Hum Genet. 1994 Nov;55(5):1042-9. Am J Hum Genet. 1994. PMID: 7977341 Free PMC article.
Is a single mutation at the same locus responsible for all affected cases in a large Alzheimer pedigree (FAD4)?
Martinez M, Campion D, Babron MC, Clerget-Darpoux F. Martinez M, et al. Among authors: babron mc. Genet Epidemiol. 1993;10(6):431-5. doi: 10.1002/gepi.1370100617. Genet Epidemiol. 1993. PMID: 8314039
Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families.
Greco L, Babron MC, Corazza GR, Percopo S, Sica R, Clot F, Fulchignoni-Lataud MC, Zavattari P, Momigliano-Richiardi P, Casari G, Gasparini P, Tosi R, Mantovani V, De Virgiliis S, Iacono G, D'Alfonso A, Selinger-Leneman H, Lemainque A, Serre JL, Clerget-Darpoux F. Greco L, et al. Among authors: babron mc. Ann Hum Genet. 2001 Jan;65(Pt 1):35-41. doi: 10.1046/j.1469-1809.2001.6510035.x. Ann Hum Genet. 2001. PMID: 11415521
Genome search in celiac disease.
Greco L, Corazza G, Babron MC, Clot F, Fulchignoni-Lataud MC, Percopo S, Zavattari P, Bouguerra F, Dib C, Tosi R, Troncone R, Ventura A, Mantavoni W, Magazzù G, Gatti R, Lazzari R, Giunta A, Perri F, Iacono G, Cardi E, de Virgiliis S, Cataldo F, De Angelis G, Musumeci S, Clerget-Darpoux F, et al. Greco L, et al. Among authors: babron mc. Am J Hum Genet. 1998 Mar;62(3):669-75. doi: 10.1086/301754. Am J Hum Genet. 1998. PMID: 9497251 Free PMC article.
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