Molina-Gomes D - Search Results

1

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

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

Lupus erythematosus proliferative glomerulonephritis in fetus.

Daïkha-Dahmane F, Bault JP, Molina-Gomes D, Hillion D, Ville Y. Daïkha-Dahmane F, et al. Lupus. 2005;14(4):326-7. doi: 10.1191/0961203303lu2045cr. Lupus. 2005. PMID: 15864920

4

Mid-trimester hyperechogenic bowel in a fetus of Japanese origin carrying a new mutation of CFTR gene (L548Q).

Yamamoto M, Molina-Gomes D, Girodon-Boulandet E, Moulis M, Leroy B, Simon-Bouy B, Selva J, Ville Y. Yamamoto M, et al. Prenat Diagn. 2006 Jan;26(1):6-8. doi: 10.1002/pd.1310. Prenat Diagn. 2006. PMID: 16378323

5

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

6

[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.

7

Gamete cytogenetic study in couples with implantation failure: aneuploidy rate is increased in both couple members.

Vialard F, Hammoud I, Molina-Gomes D, Wainer R, Bergere M, Albert M, Bailly M, de Mazancourt P, Selva J. Vialard F, et al. J Assist Reprod Genet. 2008 Nov-Dec;25(11-12):539-45. doi: 10.1007/s10815-008-9258-6. Epub 2008 Oct 30. J Assist Reprod Genet. 2008. PMID: 18972203 Free PMC article.

8

Preconceptional diagnosis for Robertsonian translocation as an alternative to preimplantation genetic diagnosis in two situations: a pilot study.

Molina Gomes D, Hammoud I, Bailly M, Bergere M, Wainer R, Selva J, Vialard F. Molina Gomes D, et al. J Assist Reprod Genet. 2009 Mar;26(2-3):113-7. doi: 10.1007/s10815-009-9293-y. Epub 2009 Jan 28. J Assist Reprod Genet. 2009. PMID: 19184396 Free PMC article.

9

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.

10

Case report: Meiotic segregation in spermatozoa of a 46,X,t(Y;10)(q11.2;p15.2) fertile translocation carrier.

Vialard F, Molina-Gomes D, Roume J, Podbiol A, Hirel C, Bailly M, Hammoud I, Dupont JM, de Mazancourt P, Selva J. Vialard F, et al. Reprod Biomed Online. 2009 Apr;18(4):549-54. doi: 10.1016/s1472-6483(10)60133-2. Reprod Biomed Online. 2009. PMID: 19400998

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