Lebbar A - Search Results

1

Is rapid aneuploidy screening used alone acceptable in prenatal diagnosis? An evaluation of the possible role of ultrasound examination.

Gaudry P, Lebbar A, Choiset A, Girard S, Lewin F, Tsatsaris V, Grangé G. Gaudry P, et al. Among authors: lebbar a. Fetal Diagn Ther. 2009;25(2):285-90. doi: 10.1159/000224429. Epub 2009 Jun 11. Fetal Diagn Ther. 2009. PMID: 19521096

2

Optimized criteria for using fluorescence in situ hybridization in the prenatal diagnosis of common aneuploidies.

Leclercq S, Lebbar A, Grange G, Tsatsaris V, Le Tessier D, Dupont JM. Leclercq S, et al. Among authors: lebbar a. Prenat Diagn. 2008 Apr;28(4):313-8. doi: 10.1002/pd.1959. Prenat Diagn. 2008. PMID: 18306148

3

Fetal loss after amniocentesis in a series of 5,780 procedures.

Gaudry P, Grangé G, Lebbar A, Choiset A, Girard S, Goffinet F, Lewin F. Gaudry P, et al. Among authors: lebbar a. Fetal Diagn Ther. 2008;23(3):217-21. doi: 10.1159/000116744. Epub 2008 Feb 20. Fetal Diagn Ther. 2008. PMID: 18417981

4

Amniocentesis performed for karyotyping after identified ultrasonographic abnormalities: what to expect?

Gaudry P, Esvan M, Meynard JB, Lebbar A, Choiset A, Lewin F, Tsatsaris V, Pannier E, Grange G. Gaudry P, et al. Among authors: lebbar a. Fetal Diagn Ther. 2012;31(1):55-62. doi: 10.1159/000330373. Epub 2011 Dec 13. Fetal Diagn Ther. 2012. PMID: 22189057

5

First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur.

Abdelhedi F, Corcos J, Cuisset L, Tsatsaris V, Tantau J, Le Tessier D, Lebbar A, Dupont JM. Abdelhedi F, et al. Among authors: lebbar a. Am J Med Genet A. 2012 Mar;158A(3):617-21. doi: 10.1002/ajmg.a.34416. Epub 2012 Feb 2. Am J Med Genet A. 2012. PMID: 22302515

6

Neonatal Silver-Russell syndrome with maternal uniparental heterodisomy, trisomy 7 mosaicism, and dysplasia of the cerebellum.

Abdelhedi F, El Khattabi L, Cuisset L, Tsatsaris V, Viot G, Druart L, Lebbar A, Dupont JM. Abdelhedi F, et al. Among authors: lebbar a. Am J Clin Pathol. 2014 Aug;142(2):248-53. doi: 10.1309/AJCPBLMPRXKU1JUE. Am J Clin Pathol. 2014. PMID: 25015868

7

Pregnancy outcome following prenatal diagnosis of an isodicentric X chromosome: first case report.

Lebbar A, Viot G, Szpiro-Tapia S, Baverel F, Rabineau D, Dupont JM. Lebbar A, et al. Prenat Diagn. 2002 Nov;22(11):973-5. doi: 10.1002/pd.444. Prenat Diagn. 2002. PMID: 12424758

8

Optical genome mapping enables constitutional chromosomal aberration detection.

Mantere T, Neveling K, Pebrel-Richard C, Benoist M, van der Zande G, Kater-Baats E, Baatout I, van Beek R, Yammine T, Oorsprong M, Hsoumi F, Olde-Weghuis D, Majdali W, Vermeulen S, Pauper M, Lebbar A, Stevens-Kroef M, Sanlaville D, Dupont JM, Smeets D, Hoischen A, Schluth-Bolard C, El Khattabi L. Mantere T, et al. Among authors: lebbar a. Am J Hum Genet. 2021 Aug 5;108(8):1409-1422. doi: 10.1016/j.ajhg.2021.05.012. Epub 2021 Jul 7. Am J Hum Genet. 2021. PMID: 34237280 Free PMC article.

9

Clonal chromosomal abnormalities identified by interphase fluorescence in situ hybridization on collagen cultured hematopoietic stem cells.

Le Tessier D, Dupont JM, Fichelson S, Bouscary D, Lebbar A, Dreyfus F, Rabineau D. Le Tessier D, et al. Among authors: lebbar a. Leukemia. 2000 May;14(5):949-50. doi: 10.1038/sj.leu.2401739. Leukemia. 2000. PMID: 10803534 No abstract available.

10

Heteromorphism 18ph+ : with or without reproductive consequences?

Tabet AC, Dupont JM, Lebbar A, Couturier-Turpin MH, Feldmann G, Rabineau D. Tabet AC, et al. Among authors: lebbar a. Ann Genet. 2001 Jul-Sep;44(3):139-42. doi: 10.1016/s0003-3995(01)01079-6. Ann Genet. 2001. PMID: 11694226

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