Boué J - Search Results

1

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome.

Oberlé I, Rousseau F, Heitz D, Kretz C, Devys D, Hanauer A, Boué J, Bertheas MF, Mandel JL. Oberlé I, et al. Among authors: boue j. Science. 1991 May 24;252(5009):1097-102. doi: 10.1126/science.252.5009.1097. Science. 1991. PMID: 2031184

2

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development.

Devys D, Biancalana V, Rousseau F, Boué J, Mandel JL, Oberlé I. Devys D, et al. Among authors: boue j. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):208-16. doi: 10.1002/ajmg.1320430134. Am J Med Genet. 1992. PMID: 1605193

3

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation.

Rousseau F, Heitz D, Biancalana V, Blumenfeld S, Kretz C, Boué J, Tommerup N, Van Der Hagen C, DeLozier-Blanchet C, Croquette MF, et al. Rousseau F, et al. Among authors: boue j. N Engl J Med. 1991 Dec 12;325(24):1673-81. doi: 10.1056/NEJM199112123252401. N Engl J Med. 1991. PMID: 1944467 Free article.

4

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: boue a, boue j. 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

5

Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic association.

Oberlé I, Boué J, Croquette MF, Voelckel MA, Mattei MG, Mandel JL. Oberlé I, et al. Among authors: boue j. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):224-31. doi: 10.1002/ajmg.1320430136. Am J Med Genet. 1992. PMID: 1605195

6

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: boue a, boue j. Am J Hum Genet. 1993 Feb;52(2):297-304. Am J Hum Genet. 1993. PMID: 8094266 Free PMC article.

7

Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome.

Oberlé I, Mandel JL, Boué J, Mattei MG, Mattei JF. Oberlé I, et al. Among authors: boue j. Lancet. 1985 Apr 13;1(8433):871. doi: 10.1016/s0140-6736(85)92228-7. Lancet. 1985. PMID: 2858726 No abstract available.

8

More precise localization of the gene for Hunter syndrome.

Le Guern E, Couillin P, Oberlé I, Ravise N, Boue J. Le Guern E, et al. Among authors: boue j. Genomics. 1990 Jul;7(3):358-62. doi: 10.1016/0888-7543(90)90169-u. Genomics. 1990. PMID: 2114352

9

Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.

Oberlé I, Heilig R, Moisan JP, Kloepfer C, Mattéi GM, Mattéi JF, Boué J, Froster-Iskenius U, Jacobs PA, Lathrop GM, et al. Oberlé I, et al. Among authors: boue j. Proc Natl Acad Sci U S A. 1986 Feb;83(4):1016-20. doi: 10.1073/pnas.83.4.1016. Proc Natl Acad Sci U S A. 1986. PMID: 3006023 Free PMC article.

10

First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe.

Boué J, Oberle I, Heilig R, Mandel JL, Moser A, Moser H, Larsen JW Jr, Dumez Y, Boué A. Boué J, et al. Among authors: boue a. Hum Genet. 1985;69(3):272-4. doi: 10.1007/BF00293039. Hum Genet. 1985. PMID: 3856557

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