Moraine C - Search Results

1

Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?

Briault S, Villard L, Rogner U, Coy J, Odent S, Lucas J, Passage E, Zhu D, Shrimpton A, Pembrey M, Till M, Guichet A, Dessay S, Fontes M, Poustka A, Moraine C. Briault S, et al. Among authors: moraine c. Am J Med Genet. 2000 Nov 13;95(2):178-81. doi: 10.1002/1096-8628(20001113)95:2<178::aid-ajmg17>3.0.co;2-v. Am J Med Genet. 2000. PMID: 11078572

2

Skewed X chromosome inactivation in carriers is not a constant finding in FG syndrome.

Raynaud M, Dessay S, Ronce N, Opitz J, Pembrey M, Romano C, Moraine C, Briault S. Raynaud M, et al. Among authors: moraine c. Eur J Hum Genet. 2003 Apr;11(4):352-6. doi: 10.1038/sj.ejhg.5200959. Eur J Hum Genet. 2003. PMID: 12700610

3

FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3].

Dessay S, Moizard MP, Gilardi JL, Opitz JM, Middleton-Price H, Pembrey M, Moraine C, Briault S. Dessay S, et al. Among authors: moraine c. Am J Med Genet. 2002 Sep 15;112(1):6-11. doi: 10.1002/ajmg.10546. Am J Med Genet. 2002. PMID: 12239712 Review.

4

X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1.

Raynaud M, Gendrot C, Dessay B, Moncla A, Ayrault AD, Moizard MP, Toutain A, Briault S, Villard L, Ronce N, Moraine C. Raynaud M, et al. Among authors: moraine c. Am J Med Genet. 1996 Jul 12;64(1):97-106. doi: 10.1002/(SICI)1096-8628(19960712)64:1<97::AID-AJMG17>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8826458

5

A gene for FG syndrome maps in the Xq12-q21.31 region.

Briault S, Hill R, Shrimpton A, Zhu D, Till M, Ronce N, Margaritte-Jeannin P, Baraitser M, Middleton-Price H, Malcolm S, Thompson E, Hoo J, Wilson G, Romano C, Guichet A, Pembrey M, Fontes M, Poustka A, Moraine C. Briault S, et al. Among authors: moraine c. Am J Med Genet. 1997 Nov 28;73(1):87-90. Am J Med Genet. 1997. PMID: 9375929

6

High resolution chromosome analysis and in situ hybridization on amniotic fluid for diagnosis of a cryptic translocation.

Guichet A, Briault S, Moraine C. Guichet A, et al. Among authors: moraine c. Prenat Diagn. 1998 Apr;18(4):399-403. Prenat Diagn. 1998. PMID: 9602490

7

Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one family.

Ronce N, Raynaud M, Toutain A, Moizard MP, Colleaux L, Gendrot C, Briault S, Moraine C. Ronce N, et al. Among authors: moraine c. Am J Med Genet. 1999 Mar 12;83(2):132-7. doi: 10.1002/(sici)1096-8628(19990312)83:2<132::aid-ajmg9>3.0.co;2-y. Am J Med Genet. 1999. PMID: 10190484

8

Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome.

Briault S, Odent S, Lucas J, Le Merrer M, Turleau C, Munnich A, Moraine C. Briault S, et al. Among authors: moraine c. Am J Med Genet. 1999 Sep 10;86(2):112-4. doi: 10.1002/(sici)1096-8628(19990910)86:2<112::aid-ajmg4>3.0.co;2-3. Am J Med Genet. 1999. PMID: 10449643

9

TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessment.

Gomot M, Ronce N, Dessay S, Zemni R, Ayrault AD, Moizard MP, Nivelon A, Gilgenkrantz S, Dourlens J, Des Portes V, Chelly J, Moraine C. Gomot M, et al. Among authors: moraine c. Am J Med Genet. 2002 Nov 1;112(4):400-4. doi: 10.1002/ajmg.10564. Am J Med Genet. 2002. PMID: 12376945

10

X-linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region.

Gendrot C, Ronce N, Toutain A, Moizard MP, Müh JP, Raynaud M, Dourlens J, Briault S, Moraine C. Gendrot C, et al. Among authors: moraine c. Clin Genet. 1994 Mar;45(3):145-53. doi: 10.1111/j.1399-0004.1994.tb04012.x. Clin Genet. 1994. PMID: 8026106

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