Goumy C - Search Results

1

[Middle interhemispheric variant of holoprosencephaly and partial 21q monosomy].

Tran Mau-Them A, Goumy C, Delabaere A, Laurichesse-Delmas H, Lemery D, Gallot D. Tran Mau-Them A, et al. Among authors: goumy c. Gynecol Obstet Fertil. 2015 Apr;43(4):326-7. doi: 10.1016/j.gyobfe.2015.02.009. Epub 2015 Mar 21. Gynecol Obstet Fertil. 2015. PMID: 25800860 French. No abstract available.

2

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. Prenat Diagn. 2004 Apr;24(4):249-56. doi: 10.1002/pd.845. Prenat Diagn. 2004. PMID: 15065097

3

Prenatal detection of mosaic isochromosome 20q: a fourth report with abnormal phenotype.

Goumy C, Beaufrère AM, Francannet C, Tchirkov A, Laurichesse Delmas H, Geissler F, Lemery D, Dechelotte PJ, Vago P. Goumy C, et al. Prenat Diagn. 2005 Aug;25(8):653-5. doi: 10.1002/pd.1216. Prenat Diagn. 2005. PMID: 16049989

4

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. Prenat Diagn. 2008 Feb;28(2):131-4. doi: 10.1002/pd.1928. Prenat Diagn. 2008. PMID: 18236428

5

Congenital diaphragmatic hernia and genital anomalies: Emanuel syndrome.

Gremeau AS, Coste K, Blanc P, Goumy C, Francannet C, Dechelotte PJ, Vago P, Laurichesse-Delmas H, Labbe A, Lemery D, Sapin V, Gallot D. Gremeau AS, et al. Among authors: goumy c. Prenat Diagn. 2009 Aug;29(8):816-8. doi: 10.1002/pd.2289. Prenat Diagn. 2009. PMID: 19434659 No abstract available.

6

Fetal skin fibroblasts: a cell model for studying the retinoid pathway in congenital diaphragmatic hernia.

Goumy C, Coste K, Marceau G, Gouas L, Tchirkov A, Vago P, Gallot D, Sapin V. Goumy C, et al. Birth Defects Res A Clin Mol Teratol. 2010 Mar;88(3):195-200. doi: 10.1002/bdra.20647. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 20063272

7

Retinoid pathway and congenital diaphragmatic hernia: hypothesis from the analysis of chromosomal abnormalities.

Goumy C, Gouas L, Marceau G, Coste K, Veronese L, Gallot D, Sapin V, Vago P, Tchirkov A. Goumy C, et al. Fetal Diagn Ther. 2010;28(3):129-39. doi: 10.1159/000313331. Epub 2010 May 26. Fetal Diagn Ther. 2010. PMID: 20501978 Free article. Review.

8

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. 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

9

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: goumy c. Morphologie. 2013 Jun;97(317):65-7. doi: 10.1016/j.morpho.2013.01.001. Epub 2013 Mar 7. Morphologie. 2013. PMID: 23473874

10

Prenatal ultrasound findings observed in the Wolf-Hirschhorn syndrome: data from the registry of congenital malformations in Auvergne.

Debost-Legrand A, Goumy C, Laurichesse-Delmas H, Déchelotte P, Beaufrère AM, Lémery D, Francannet C, Gallot D. Debost-Legrand A, et al. Among authors: goumy c. Birth Defects Res A Clin Mol Teratol. 2013 Dec;97(12):806-11. doi: 10.1002/bdra.23194. Epub 2013 Nov 6. Birth Defects Res A Clin Mol Teratol. 2013. PMID: 24343879

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