Demaille J - Search Results

1

Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation.

Lefort G, Blanchet P, Chaze AM, Girardet A, Sarda P, Demaille J, Pellestor F. Lefort G, et al. Among authors: demaille j. J Med Genet. 2001 Jan;38(1):67-73. doi: 10.1136/jmg.38.1.67. J Med Genet. 2001. PMID: 11334011 Free PMC article. No abstract available.

2

Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.

Lefort G, Blanchet P, Belgrade N, Rivier F, Chaze AM, Sarda P, Demaille J, Pellestor F. Lefort G, et al. Among authors: demaille j. Am J Med Genet. 2002 Dec 15;113(4):333-8. doi: 10.1002/ajmg.b.10720. Am J Med Genet. 2002. Corrected and republished in: Am J Med Genet A. 2003 Apr 15;118A(2):333-8. PMID: 12457404 Corrected and republished.

3

Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.

Lefort G, Blanchet P, Belgrade N, Rivier F, Chaze AM, Sarda P, Demaille J, Pellestor F. Lefort G, et al. Among authors: demaille j. Am J Med Genet A. 2003 Apr 15;118A(2):333-8. Am J Med Genet A. 2003. PMID: 12698965

4

Maternal aging and chromosomal abnormalities: new data drawn from in vitro unfertilized human oocytes.

Pellestor F, Andréo B, Arnal F, Humeau C, Demaille J. Pellestor F, et al. Among authors: demaille j. Hum Genet. 2003 Feb;112(2):195-203. doi: 10.1007/s00439-002-0852-x. Epub 2002 Oct 29. Hum Genet. 2003. PMID: 12522562

5

Sequential multiple probe fluorescence in-situ hybridization analysis of human oocytes and polar bodies by combining centromeric labelling and whole chromosome painting.

Anahory T, Andréo B, Régnier-Vigouroux G, Soulie JP, Baudouin M, Demaille J, Pellestor F. Anahory T, et al. Among authors: demaille j. Mol Hum Reprod. 2003 Oct;9(10):577-85. doi: 10.1093/molehr/gag075. Mol Hum Reprod. 2003. PMID: 12970395

6

Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation test.

Tuffery S, Chambert S, Bareil C, Sarda P, Coubes C, Echenne B, Demaille J, Claustres M. Tuffery S, et al. Among authors: demaille j. Hum Genet. 1998 Mar;102(3):334-42. doi: 10.1007/s004390050702. Hum Genet. 1998. PMID: 9544849

7

Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.

Tuffery S, Moine P, Sarda P, Lefort G, Boulot P, Demaille J, Claustres M. Tuffery S, et al. Among authors: demaille j. Genet Couns. 1994;5(2):183-5. Genet Couns. 1994. PMID: 7917130

8

First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markers.

Girardet A, Hamamah S, Anahory T, Déchaud H, Sarda P, Hédon B, Demaille J, Claustres M. Girardet A, et al. Among authors: demaille j. Mol Hum Reprod. 2003 Feb;9(2):111-6. doi: 10.1093/molehr/gag014. Mol Hum Reprod. 2003. PMID: 12569181

9

Mechanisms of non-disjunction in human female meiosis: the co-existence of two modes of malsegregation evidenced by the karyotyping of 1397 in-vitro unfertilized oocytes.

Pellestor F, Andréo B, Arnal F, Humeau C, Demaille J. Pellestor F, et al. Among authors: demaille j. Hum Reprod. 2002 Aug;17(8):2134-45. doi: 10.1093/humrep/17.8.2134. Hum Reprod. 2002. PMID: 12151449

10

Fast multicolor primed in situ protocol for chromosome identification in isolated cells may be used for human oocytes and polar bodies.

Pellestor F, Anahory T, Andréo B, Régnier-Vigouroux G, Soulié JP, Baudouin M, Demaille J. Pellestor F, et al. Among authors: demaille j. Fertil Steril. 2004 Feb;81(2):408-15. doi: 10.1016/j.fertnstert.2003.08.014. Fertil Steril. 2004. PMID: 14967382 Free article.

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