Bonaïti-Pellié C - Search Results

1

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. Nat Genet. 1994 Nov;8(3):264-8. doi: 10.1038/ng1194-264. Nat Genet. 1994. PMID: 7632217 Free PMC article.

2

Reply to "The question of heterogeneity in Marfan syndrome".

Boileau C, Junien C, Collod G, Jondeau G, Dubourg O, Bourdarias JP, Bonaïti-Pellié C, Frezal J, Maroteaux P. Boileau C, et al. Nat Genet. 1995 Mar;9(3):230-231. doi: 10.1038/ng0395-230. Nat Genet. 1995. PMID: 21836810 Free PMC article. No abstract available.

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

Linkage detection by the Affected-Pedigree-Member method: what is really tested?

Babron MC, Martinez M, Bonaïti-Pellié C, Clerget-Darpoux F. Babron MC, et al. Genet Epidemiol. 1993;10(6):389-94. doi: 10.1002/gepi.1370100610. Genet Epidemiol. 1993. PMID: 8314032

5

Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defects.

Saint-Jore B, Varret M, Dachet C, Rabès JP, Devillers M, Erlich D, Blanchard P, Krempf M, Mathé D, Chanu B, Jacotot B, Farnier M, Bonaïti-Péllié C, Junien C, Boileau C. Saint-Jore B, et al. Eur J Hum Genet. 2000 Aug;8(8):621-30. doi: 10.1038/sj.ejhg.5200516. Eur J Hum Genet. 2000. PMID: 10952765

6

Assessing the effect of multiple linkage tests in complex diseases.

Clerget-Darpoux F, Babron MC, Bonaïti-Pellié C. Clerget-Darpoux F, et al. Genet Epidemiol. 1990;7(4):245-53. doi: 10.1002/gepi.1370070403. Genet Epidemiol. 1990. PMID: 2227371

7

Hereditary retinoblastoma: can balanced insertion entirely explain the differences of expressivity among families?

Bonaïti-Pellié C, Clerget-Darpoux F, Babron MC. Bonaïti-Pellié C, et al. Hum Genet. 1990 Dec;86(2):203-8. doi: 10.1007/BF00197706. Hum Genet. 1990. PMID: 2265833

8

The Gm-Pi linkage in 843 French families: effect of the alleles Pi Z and Pi S.

Babron MC, Constans J, Dugoujon JM, Cambon-Thomsen A, Bonaïti-Pellié C. Babron MC, et al. Ann Hum Genet. 1990 May;54(2):107-13. doi: 10.1111/j.1469-1809.1990.tb00366.x. Ann Hum Genet. 1990. PMID: 2382967

9

Mapping of a susceptibility locus for Crohn's disease on chromosome 16.

Hugot JP, Laurent-Puig P, Gower-Rousseau C, Olson JM, Lee JC, Beaugerie L, Naom I, Dupas JL, Van Gossum A, Orholm M, Bonaiti-Pellie C, Weissenbach J, Mathew CG, Lennard-Jones JE, Cortot A, Colombel JF, Thomas G. Hugot JP, et al. Nature. 1996 Feb 29;379(6568):821-3. doi: 10.1038/379821a0. Nature. 1996. PMID: 8587604

10

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

Moutou C, Junien C, Henry I, Bonaïti-Pellié C. Moutou C, et al. J Med Genet. 1992 Apr;29(4):217-20. doi: 10.1136/jmg.29.4.217. J Med Genet. 1992. PMID: 1583638 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

143 results

Search Page

Filters