Mornet E - Search Results

1

Direct DNA analysis of fragile X syndrome in Spanish pedigrees.

Tejada I, Mornet E, Biancalana V, Oberlé I, Boué J, Mandel JL, Boué A. Tejada I, et al. Among authors: mornet e. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):282-90. doi: 10.1002/ajmg.1320430144. Am J Med Genet. 1992. PMID: 1351363

2

Affected sibs with fragile X syndrome exhibit an age-dependent decrease in the size of the fragile X full mutation.

Mornet E, Jokic M, Bogyo A, Tejada I, Deluchat C, Boué J, Boué A. Mornet E, et al. Clin Genet. 1993 Mar;43(3):157-9. doi: 10.1111/j.1399-0004.1993.tb04462.x. Clin Genet. 1993. PMID: 8098999

3

Identification by molecular diagnosis of mosaic Turner's syndrome in an obligate carrier female for fragile X syndrome.

Tejada MI, Mornet E, Tizzano E, Molina M, Baiget M, Boue A. Tejada MI, et al. Among authors: mornet e. J Med Genet. 1994 Jan;31(1):76-8. doi: 10.1136/jmg.31.1.76. J Med Genet. 1994. PMID: 8151646 Free PMC article.

4

A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.

Rousseau F, Heitz D, Tarleton J, MacPherson J, Malmgren H, Dahl N, Barnicoat A, Mathew C, Mornet E, Tejada I, et al. Rousseau F, et al. Among authors: mornet e. Am J Hum Genet. 1994 Aug;55(2):225-37. Am J Hum Genet. 1994. PMID: 8037202 Free PMC article. Clinical Trial.

5

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.

6

Molecular analysis of a ring chromosome X in a family with fragile X syndrome.

Mornet E, Bogyo A, Deluchat C, Simon-Bouy B, Mathieu M, Thépot F, Grisard MC, Leguern E, Boué J, Boué A. Mornet E, et al. Hum Genet. 1993 Oct;92(4):373-8. doi: 10.1007/BF01247338. Hum Genet. 1993. PMID: 8225318

7

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

8

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

9

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

10

Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency.

Mornet E, Crété P, Kuttenn F, Raux-Demay MC, Boué J, White PC, Boué A. Mornet E, et al. Am J Hum Genet. 1991 Jan;48(1):79-88. Am J Hum Genet. 1991. PMID: 1985465 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

132 results

Search Page

Filters