Oberlé I - Search Results

1

New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA interval.

Oberlé I, Vincent A, Abbadi N, Rousseau F, Hupkes PE, Hors-Cayla MC, Gilgenkrantz S, Oostra BA, Mandel JL. Oberlé I, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):336-42. doi: 10.1002/ajmg.1320380234. Am J Med Genet. 1991. PMID: 1673307

2

On some technical aspects of direct DNA diagnosis of the fragile X syndrome.

Rousseau F, Heitz D, Biancalana V, Oberlé I, Mandel JL. Rousseau F, et al. Among authors: oberle i. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):197-207. doi: 10.1002/ajmg.1320430133. Am J Med Genet. 1992. PMID: 1351361

3

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis.

Vincent A, Heitz D, Petit C, Kretz C, Oberlé I, Mandel JL. Vincent A, et al. Among authors: oberle i. Nature. 1991 Feb 14;349(6310):624-6. doi: 10.1038/349624a0. Nature. 1991. PMID: 1672039

4

Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation.

Rousseau F, Heitz D, Oberlé I, Mandel JL. Rousseau F, et al. Among authors: oberle i. J Med Genet. 1991 Dec;28(12):830-6. doi: 10.1136/jmg.28.12.830. J Med Genet. 1991. PMID: 1757958 Free PMC article.

5

New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locus.

Rousseau F, Vincent A, Oberlé I, Mandel JL. Rousseau F, et al. Among authors: oberle i. Hum Genet. 1990 Feb;84(3):263-6. doi: 10.1007/BF00200572. Hum Genet. 1990. PMID: 1968034

6

Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome.

Feil R, Palmieri G, d'Urso M, Heilig R, Oberlé I, Mandel JL. Feil R, et al. Among authors: oberle i. Am J Hum Genet. 1990 Apr;46(4):720-8. Am J Hum Genet. 1990. PMID: 1969226 Free PMC article.

7

A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome.

Vincent A, Kretz C, Oberlé I, Mandel JL. Vincent A, et al. Among authors: oberle i. Hum Genet. 1989 Apr;82(1):85-6. doi: 10.1007/BF00288280. Hum Genet. 1989. PMID: 2565870

8

The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.

Vincent A, Dahl N, Oberlé I, Hanauer A, Mandel JL, Malmgren H, Pettersson U. Vincent A, et al. Among authors: oberle i. Genomics. 1989 Nov;5(4):797-801. doi: 10.1016/0888-7543(89)90121-3. Genomics. 1989. PMID: 2574147

9

Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome.

Arveiler B, Oberlé I, Mandel JL. Arveiler B, et al. Among authors: oberle i. Genomics. 1987 Sep;1(1):60-6. doi: 10.1016/0888-7543(87)90105-4. Genomics. 1987. PMID: 2889662

10

Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.

Arveiler B, Oberlé I, Vincent A, Hofker MH, Pearson PL, Mandel JL. Arveiler B, et al. Among authors: oberle i. Am J Hum Genet. 1988 Feb;42(2):380-9. Am J Hum Genet. 1988. PMID: 2893549 Free PMC article.

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