Vago P - Search Results

1

Spatial organization of chromosome territories in the interphase nucleus of trisomy 21 cells.

Kemeny S, Tatout C, Salaun G, Pebrel-Richard C, Goumy C, Ollier N, Maurin E, Pereira B, Vago P, Gouas L. Kemeny S, et al. Among authors: vago p. Chromosoma. 2018 Jun;127(2):247-259. doi: 10.1007/s00412-017-0653-6. Epub 2017 Dec 14. Chromosoma. 2018. PMID: 29238858

2

Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p.

Goumy C, Beaufrère AM, Tchirkov A, Gouas L, Gaspard F, Giollant M, Roucaute T, Veronèse L, Lemery D, Vago P. Goumy C, et al. Among authors: vago p. Prenat Diagn. 2008 Feb;28(2):131-4. doi: 10.1002/pd.1928. Prenat Diagn. 2008. PMID: 18236428

3

[Trisomy 21 and cancers].

Ayed W, Gouas L, Penault-Llorca F, Amouri A, Tchirkov A, Vago P. Ayed W, et al. Among authors: vago p. Morphologie. 2012 Oct;96(314-315):57-66. doi: 10.1016/j.morpho.2012.10.001. Epub 2012 Nov 7. Morphologie. 2012. PMID: 23141635 Review. French.

4

Characterization by microarray and meiotic segregation study of a der(10)t(10;18) in a patient with infertility and normal phenotype.

Kemeny S, Brugnon F, Eymard-Pierre E, Goumy C, Janny L, Tchirkov A, Francannet C, Vago P, Pebrel-Richard C. Kemeny S, et al. Among authors: vago p. Asian J Androl. 2017 Jan-Feb;19(1):135-137. doi: 10.4103/1008-682X.172818. Asian J Androl. 2017. PMID: 26975482 Free PMC article. No abstract available.

5

Sperm meiotic segregation of a balanced interchromosomal reciprocal insertion resulting in recurrent spontaneous miscarriage.

Salaun G, Tchirkov A, Francannet C, Pons H, Brugnon F, Pebrel-Richard C, Gouas L, Eymard-Pierre E, Vago P, Goumy C. Salaun G, et al. Among authors: vago p. Reprod Biomed Online. 2018 Jul;37(1):100-106. doi: 10.1016/j.rbmo.2018.03.019. Epub 2018 Apr 9. Reprod Biomed Online. 2018. PMID: 29680196

6

Gene dosage methods as diagnostic tools for the identification of chromosome abnormalities.

Gouas L, Goumy C, Véronèse L, Tchirkov A, Vago P. Gouas L, et al. Among authors: vago p. Pathol Biol (Paris). 2008 Sep;56(6):345-53. doi: 10.1016/j.patbio.2008.03.010. Epub 2008 Jun 2. Pathol Biol (Paris). 2008. PMID: 18513889 Review.

7

Prenatal diagnosis of a rare de novo centromeric chromosome 6 variant.

Goumy C, Kemeny S, Eymard-Pierre E, Richard C, Gouas L, Combes P, Gay-Bellile M, Gallot D, Tchirkov A, Vago P. Goumy C, et al. Among authors: vago p. Gene. 2011 Dec 15;490(1-2):15-7. doi: 10.1016/j.gene.2011.09.008. Epub 2011 Oct 1. Gene. 2011. PMID: 21989483

8

Prenatal ultrasound diagnosis of a 48,XXYY syndrome.

Kemeny S, Pebrel-Richard C, Gouas L, Veronese L, Lemery D, Tchirkov A, Goumy C, Vago P. Kemeny S, et al. Among authors: vago p. Morphologie. 2013 Jun;97(317):65-7. doi: 10.1016/j.morpho.2013.01.001. Epub 2013 Mar 7. Morphologie. 2013. PMID: 23473874

9

Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosis.

Goumy C, Bonnet-Dupeyron MN, Cherasse Y, Laurichesse H, Jaffray JY, Lacroute G, Geneix A, Lemery D, Vago P. Goumy C, et al. Among authors: vago p. Prenat Diagn. 2004 Apr;24(4):249-56. doi: 10.1002/pd.845. Prenat Diagn. 2004. PMID: 15065097

10

Trisomy 20q caused by interstitial duplication 20q13.2: clinical report and literature review.

Blanc P, Gouas L, Francannet C, Giollant M, Vago P, Goumy C. Blanc P, et al. Among authors: vago p. Am J Med Genet A. 2008 May 15;146A(10):1307-11. doi: 10.1002/ajmg.a.32278. Am J Med Genet A. 2008. PMID: 18384146 Review.

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