Molina-Gomes D - Search Results

1

Prenatal diagnosis of 24 cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations.

Dupont C, Grati FR, Choy KW, Jaillard S, Toutain J, Maurin ML, Martínez-Conejero JA, Beneteau C, Coussement A, Molina-Gomes D, Horelli-Kuitunen N, Aboura A, Tabet AC, Besseau-Ayasse J, Bessieres-Grattagliano B, Simoni G, Ayala G, Benzacken B, Vialard F. Dupont C, et al. Prenat Diagn. 2015 Jan;35(1):35-43. doi: 10.1002/pd.4478. Epub 2014 Sep 16. Prenat Diagn. 2015. PMID: 25118001

2

Dandy-Walker syndrome and corpus callosum agenesis in 5p deletion.

Vialard F, Robyr R, Hillion Y, Molina Gomes D, Selva J, Ville Y. Vialard F, et al. Prenat Diagn. 2005 Apr;25(4):311-3. doi: 10.1002/pd.1130. Prenat Diagn. 2005. PMID: 15849798

3

Partial trisomy 20p resulting from recombination of a maternal pericentric inversion: case report of a prenatal diagnosis by chorionic villus sampling.

Molina-Gomes D, Nebout V, Daikha-Dahmane F, Vialard F, Ville Y, Selva J. Molina-Gomes D, et al. Prenat Diagn. 2006 Mar;26(3):239-41. doi: 10.1002/pd.1389. Prenat Diagn. 2006. PMID: 16485319

4

[Contribution of first polar body analysis to understanding of human aneuploidy mechanism].

Selva J, Bergere M, Molina-Gomes D, Hammoud I, Lombroso R, Vialard F. Selva J, et al. Bull Acad Natl Med. 2005 Nov;189(8):1761-72; discussion 1772. Bull Acad Natl Med. 2005. PMID: 16737101 Review. French.

5

Partial chromosome deletion: a new trisomy rescue mechanism?

Vialard F, Molina-Gomes D, Quarello E, Leroy B, Ville Y, Selva J. Vialard F, et al. Fetal Diagn Ther. 2009;25(1):111-4. doi: 10.1159/000203400. Epub 2009 Feb 25. Fetal Diagn Ther. 2009. PMID: 19246929

6

Fetal karyotype in feto-fetal transfusion syndrome: a 7-year experience.

Vialard F, Salomon LJ, Winer N, Bussières L, Molina Gomes D, Ville Y. Vialard F, et al. Prenat Diagn. 2009 Aug;29(8):804-5. doi: 10.1002/pd.2272. Prenat Diagn. 2009. PMID: 19399755 No abstract available.

7

Array comparative genomic hybridization in prenatal diagnosis: another experience.

Vialard F, Molina Gomes D, Leroy B, Quarello E, Escalona A, Le Sciellour C, Serazin V, Roume J, Ville Y, de Mazancourt P, Selva J. Vialard F, et al. Fetal Diagn Ther. 2009;25(2):277-84. doi: 10.1159/000224112. Epub 2009 Jun 11. Fetal Diagn Ther. 2009. PMID: 19521095

8

[New technologies for genome analysis: Which use in prenatal diagnosis].

Vialard F, Molina Gomes D. Vialard F, et al. Gynecol Obstet Fertil. 2011 Jan;39(1):32-41. doi: 10.1016/j.gyobfe.2010.09.006. Epub 2010 Dec 24. Gynecol Obstet Fertil. 2011. PMID: 21185761 French.

9

Prenatal BACs-on-Beads™ : a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis.

Vialard F, Simoni G, Aboura A, De Toffol S, Molina Gomes D, Marcato L, Serero S, Clement P, Bouhanna P, Rouleau E, Grimi B, Selva J, Gaetani E, Maggi F, Joseph A, Benzacken B, Grati FR. Vialard F, et al. Prenat Diagn. 2011 May;31(5):500-8. doi: 10.1002/pd.2727. Epub 2011 Mar 14. Prenat Diagn. 2011. PMID: 21404304

10

Williams-Beuren syndrome: the prenatal phenotype.

Popowski T, Vialard F, Leroy B, Bault JP, Molina-Gomes D. Popowski T, et al. Am J Obstet Gynecol. 2011 Dec;205(6):e6-8. doi: 10.1016/j.ajog.2011.09.017. Epub 2011 Sep 24. Am J Obstet Gynecol. 2011. PMID: 22000898

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

56 results

Search Page

Filters