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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: coulon m. Am J Hum Genet. 1993 Jul;53(1):46-54. Am J Hum Genet. 1993. PMID: 8317497 Free PMC article.
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: coulon m. Eur J Hum Genet. 1996;4(5):292-5. doi: 10.1159/000472216. Eur J Hum Genet. 1996. PMID: 8946175
[Marfan syndrome. Current molecular data].
Boileau C, Coulon M, Junien C. Boileau C, et al. Among authors: coulon m. Arch Fr Pediatr. 1992 Dec;49(10):941-3. Arch Fr Pediatr. 1992. PMID: 1304168 Review. French. No abstract available.
Linkage analysis of five fibrillar collagen loci in a large French Marfan syndrome family.
Boileau C, Jondeau G, Bonaiti C, Coulon M, Delorme G, Dubourg O, Bourdarias JP, Junien C. Boileau C, et al. Among authors: coulon m. J Med Genet. 1990 Feb;27(2):78-81. doi: 10.1136/jmg.27.2.78. J Med Genet. 1990. PMID: 1969488 Free PMC article.
Demonstration of the recurrence of Marfan-like skeletal and cardiovascular manifestations due to germline mosaicism for an FBN1 mutation.
Collod-Béroud G, Lackmy-Port-Lys M, Jondeau G, Mathieu M, Maingourd Y, Coulon M, Guillotel M, Junien C, Boileau C. Collod-Béroud G, et al. Among authors: coulon m. Am J Hum Genet. 1999 Sep;65(3):917-21. doi: 10.1086/302545. Am J Hum Genet. 1999. PMID: 10441597 Free PMC article. No abstract available.
A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32.
Varret M, Rabès JP, Saint-Jore B, Cenarro A, Marinoni JC, Civeira F, Devillers M, Krempf M, Coulon M, Thiart R, Kotze MJ, Schmidt H, Buzzi JC, Kostner GM, Bertolini S, Pocovi M, Rosa A, Farnier M, Martinez M, Junien C, Boileau C. Varret M, et al. Among authors: coulon m. Am J Hum Genet. 1999 May;64(5):1378-87. doi: 10.1086/302370. Am J Hum Genet. 1999. PMID: 10205269 Free PMC article.
Extended haplotypes and linkage disequilibrium between 11 markers at the APOA1-C3-A4 gene cluster on chromosome 11.
Benlian P, Boileau C, Loux N, Pastier D, Masliah J, Coulon M, Nigou M, Ragab A, Guimard J, Ruidavets JB, et al. Benlian P, et al. Among authors: coulon m. Am J Hum Genet. 1991 May;48(5):903-10. Am J Hum Genet. 1991. PMID: 1673288 Free PMC article.
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: coulon m. Nat Genet. 1994 Nov;8(3):264-8. doi: 10.1038/ng1194-264. Nat Genet. 1994. PMID: 7632217 Free PMC article.
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Kunkel LM, Hejtmancik JF, Caskey CT, Speer A, Monaco AP, Middlesworth W, Colletti CA, Bertelson C, Müller U, Bresnan M, Shapiro F, Tantravahi U, Speer J, Latt SA, Bartlett R, Pericak-Vance MA, Roses AD, Thompson MW, Ray PN, Worton RG, Fischbeck KH, Gallano P, Coulon M, Duros C, Boue J, Junien C, Chelly J, Hamard G, Jeanpierre M, Lambert M, Kaplan JC, Emery A, Dorkins H, McGlade S, Davies KE, Boehm C, Arveiler B, Lemaire C, Morgan GJ, Denton MJ, Amos J, Bobrow M, Benham F, Boswinkel E, Cole C, Dubowitz V, Hart K, Hodgson S, Johnson L, Walker A, Roncuzzi L, Ferlini A, Nobile C, Romeo G, Wilcox DE, Affara NA, Ferguson-Smith MA, Lindolf M, Kaariainen H, de la Chapelle A, Ionasescu V, Searby C, Ionasescu R, Bakker E, van Ommen GJ, Pearson PL, Greenberg CR, Hamerton JL, Wrogemann K, Doherty RA, Polakowska R, Hyser C, Quirk S, Thomas N, Harper JF, Darras BT, Francke U. Kunkel LM, et al. Among authors: coulon m. Nature. 1986 Jul 3-9;322(6074):73-7. doi: 10.1038/322073a0. Nature. 1986. PMID: 3014348
[Molecular diagnosis of Duchenne and Becker muscular dystrophies. Current data].
Junien C, Boué J, Duros C, Coulon M, Cohen P, Dehaupas I, Gallano P, Léotard B, Nicolas H, Boué A. Junien C, et al. Among authors: coulon m. Ann Genet. 1987;30(1):5-16. Ann Genet. 1987. PMID: 3498430 French.
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