Taillandier A - 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: taillandier a. Hum Genet. 1990 Apr;84(5):449-54. doi: 10.1007/BF00195818. Hum Genet. 1990. PMID: 1969843

2

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: taillandier a. Clin Genet. 1991 Apr;39(4):304-5. doi: 10.1111/j.1399-0004.1991.tb03030.x. Clin Genet. 1991. PMID: 1712680

3

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: taillandier a. Clin Genet. 1991 Sep;40(3):218-24. doi: 10.1111/j.1399-0004.1991.tb03080.x. Clin Genet. 1991. PMID: 1723032

4

Genotyping of the Spanish cystic fibrosis population at the delta F508 mutation site and RFLP linked loci.

Jaume-Roig B, Simon-Bouy B, Taillandier A, Serre JL, Antich J, Bellon J, Boué J, Boué A. Jaume-Roig B, et al. Among authors: taillandier a. Hum Genet. 1990 Sep;85(4):410-1. doi: 10.1007/BF02428284. Hum Genet. 1990. PMID: 1976593

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: taillandier a. 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. Among authors: taillandier a. Clin Genet. 1989 Feb;35(2):81-7. doi: 10.1111/j.1399-0004.1989.tb02911.x. Clin Genet. 1989. PMID: 2566403

7

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. Among authors: taillandier a. 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

8

Nearly 80% of cystic fibrosis heterozygotes and 64% of couples at risk may be detected through a unique screening of four mutations by ASO reverse dot blot.

Serre JL, Taillandier A, Mornet E, Simon-Bouy B, Boué J, Boué A. Serre JL, et al. Among authors: taillandier a. Genomics. 1991 Dec;11(4):1149-51. doi: 10.1016/0888-7543(91)90043-e. Genomics. 1991. PMID: 1783382

9

Transition from normal to premutated alleles in fragile X syndrome results from a multistep process.

Montagnon M, Bogyo A, Deluchat C, Jokic M, Chateau C, Taillandier A, Thomas F, Simon-Bouy B, Boué J, Serre JL, et al. Montagnon M, et al. Among authors: taillandier a. Eur J Hum Genet. 1994;2(2):125-31. doi: 10.1159/000472352. Eur J Hum Genet. 1994. PMID: 8044657

10

Analysis of germline variation at the FMR1 CGG repeat shows variation in the normal-premutated borderline range.

Mornet E, Chateau C, Hirst MC, Thepot F, Taillandier A, Cibois O, Serre JL. Mornet E, et al. Among authors: taillandier a. Hum Mol Genet. 1996 Jun;5(6):821-5. doi: 10.1093/hmg/5.6.821. Hum Mol Genet. 1996. PMID: 8776598

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