Mornet E - Search Results

1

Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations genetics.

Serre JL, Simon-Bouy B, Mornet E, Jaume-Roig B, Balassopoulou A, Schwartz M, Taillandier A, Boué J, Boué A. Serre JL, et al. Among authors: mornet e. Hum Genet. 1990 Apr;84(5):449-54. doi: 10.1007/BF00195818. Hum Genet. 1990. PMID: 1969843

2

Carrier detection and prenatal diagnosis of cystic fibrosis using an intragenic TA-repeat polymorphism.

Mornet E, Chateau C, Simon-Bouy B, Boue J, Zielenski J, Tsui LC, Boue A. Mornet E, et al. Hum Genet. 1992 Feb;88(4):479-81. doi: 10.1007/BF00215687. Hum Genet. 1992. PMID: 1371264

3

The delta F508 mutation in mild adult forms of cystic fibrosis (CF).

Simon-Bouy B, Mornet E, Taillandier A, Serre JL, Boue J, Boue A. Simon-Bouy B, et al. Among authors: mornet e. Clin Genet. 1991 Apr;39(4):304-5. doi: 10.1111/j.1399-0004.1991.tb03030.x. Clin Genet. 1991. PMID: 1712680

4

Nine mutations in the cystic fibrosis (CF) gene account for 80% of the CF chromosomes in French patients.

Simon-Bouy B, Mornet E, Serre JL, Taillandier A, Boué J, Boué A. Simon-Bouy B, et al. Among authors: mornet e. Clin Genet. 1991 Sep;40(3):218-24. doi: 10.1111/j.1399-0004.1991.tb03080.x. Clin Genet. 1991. PMID: 1723032

5

The cystic fibrosis delta F508 mutation in the French population.

Simon-Bouy B, Mornet E, Serre JL, Taillandier A, Boué J, Boué A. Simon-Bouy B, et al. Among authors: mornet e. Hum Genet. 1990 Sep;85(4):431-2. doi: 10.1007/BF02428300. Hum Genet. 1990. PMID: 2210765

6

Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probes.

Mornet E, Simon-Bouy B, Serre JL, Muller F, Taillandier A, Martinez M, Boue J, Boue A. Mornet E, et al. Clin Genet. 1989 Feb;35(2):81-7. doi: 10.1111/j.1399-0004.1989.tb02911.x. Clin Genet. 1989. PMID: 2566403

7

Genetic differences between cystic fibrosis with and without meconium ileus.

Mornet E, Simon-Bouy B, Serre JL, Estivill X, Farrall M, Williamson R, Boue J, Boue A. Mornet E, et al. Lancet. 1988 Feb 20;1(8582):376-8. doi: 10.1016/s0140-6736(88)91180-4. Lancet. 1988. PMID: 2893188

8

General cystic fibrosis mutations are usually missense mutations affecting two specific protein domains and associated with a specific RFLP marker haplotype.

Serre JL, Mornet E, Simon-Bouy B, Boué J, Boué A. Serre JL, et al. Among authors: mornet e. Eur J Hum Genet. 1993;1(4):287-95. doi: 10.1159/000472426. Eur J Hum Genet. 1993. PMID: 7521765

9

Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes.

Oudet C, Mornet E, Serre JL, Thomas F, Lentes-Zengerling S, Kretz C, Deluchat C, Tejada I, Boué J, Boué A, et al. Oudet C, et al. Among authors: mornet e. Am J Hum Genet. 1993 Feb;52(2):297-304. Am J Hum Genet. 1993. PMID: 8094266 Free PMC article.

10

A molecular-based estimation of the prevalence of hypophosphatasia in the European population.

Mornet E, Yvard A, Taillandier A, Fauvert D, Simon-Bouy B. Mornet E, et al. Ann Hum Genet. 2011 May;75(3):439-45. doi: 10.1111/j.1469-1809.2011.00642.x. Epub 2011 Mar 24. Ann Hum Genet. 2011. PMID: 21488855

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