Boileau C - Search Results

1

[Contribution of genetics to pathogenicity and diagnosis of Marfan syndrome].

Boileau C, Collod G, Bonnet D. Boileau C, et al. Arch Mal Coeur Vaiss. 1997 Dec;90(12 Suppl):1707-12. Arch Mal Coeur Vaiss. 1997. PMID: 9587455 French.

2

A second locus for Marfan syndrome maps to chromosome 3p24.2-p25.

Collod G, Babron MC, Jondeau G, Coulon M, Weissenbach J, Dubourg O, Bourdarias JP, Bonaïti-Pellié C, Junien C, Boileau C. Collod G, et al. Among authors: boileau c. Nat Genet. 1994 Nov;8(3):264-8. doi: 10.1038/ng1194-264. Nat Genet. 1994. PMID: 7632217 Free PMC article.

3

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. Am J Hum Genet. 1993 Jul;53(1):46-54. Am J Hum Genet. 1993. PMID: 8317497 Free PMC article.

4

Identification of the haplotype associated with the APOB-3500 mutation in a French hypercholesterolemic subject: further support for a unique European ancestral mutation.

Loux N, Saint-Jore B, Collod G, Benlian P, Cambou JP, Denat M, Junien C, Boileau C. Loux N, et al. Among authors: boileau c. Hum Mutat. 1993;2(2):145-7. doi: 10.1002/humu.1380020216. Hum Mutat. 1993. PMID: 8318993 No abstract available.

5

Software and database for the analysis of mutations in the human FBN1 gene.

Collod G, Béroud C, Soussi T, Junien C, Boileau C. Collod G, et al. Among authors: boileau c. Nucleic Acids Res. 1996 Jan 1;24(1):137-40. doi: 10.1093/nar/24.1.137. Nucleic Acids Res. 1996. PMID: 8594563 Free PMC article.

6

Fibulin-2: genetic mapping and exclusion as a candidate gene in Marfan syndrome type 2.

Collod G, Chu ML, Sasaki T, Coulon M, Timpl R, Renkart L, Weissenbach J, Jondeau G, Bourdarias JP, Junien C, Boileau C. Collod G, et al. Among authors: boileau c. Eur J Hum Genet. 1996;4(5):292-5. doi: 10.1159/000472216. Eur J Hum Genet. 1996. PMID: 8946175 Free article.

7

Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene.

Collod-Béroud G, Béroud C, Adès L, Black C, Boxer M, Brock DJ, Godfrey M, Hayward C, Karttunen L, Milewicz D, Peltonen L, Richards RI, Wang M, Junien C, Boileau C. Collod-Béroud G, et al. Among authors: boileau c. Nucleic Acids Res. 1997 Jan 1;25(1):147-50. doi: 10.1093/nar/25.1.147. Nucleic Acids Res. 1997. PMID: 9016526 Free PMC article.

8

Marfan Database (third edition): new mutations and new routines for the software.

Collod-Béroud G, Béroud C, Ades L, Black C, Boxer M, Brock DJ, Holman KJ, de Paepe A, Francke U, Grau U, Hayward C, Klein HG, Liu W, Nuytinck L, Peltonen L, Alvarez Perez AB, Rantamäki T, Junien C, Boileau C. Collod-Béroud G, et al. Among authors: boileau c. Nucleic Acids Res. 1998 Jan 1;26(1):229-3. doi: 10.1093/nar/26.1.229. Nucleic Acids Res. 1998. PMID: 9399842 Free PMC article.

9

Marfan syndrome and fibrillin disorders.

Le Parc JM, Molcard S, Tubach F, Boileau C, Jondeau G, Muti C, Chevallier B, Pisella PJ. Le Parc JM, et al. Among authors: boileau c. Joint Bone Spine. 2000;67(5):401-7. Joint Bone Spine. 2000. PMID: 11143906 Review.

10

Marfan syndrome in the third Millennium.

Collod-Béroud G, Boileau C. Collod-Béroud G, et al. Among authors: boileau c. Eur J Hum Genet. 2002 Nov;10(11):673-81. doi: 10.1038/sj.ejhg.5200876. Eur J Hum Genet. 2002. PMID: 12404097 Free PMC article. Review.

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