Druart L - Search Results

1

Interstitial deletion 6p22.3-p24.3 characterized by CGH array in a foetus with multiple malformations.

Colmant C, Brisset S, Tachdjian G, Gautier V, Ftouki M, Laroudie M, Druart L, Frydman R, Picone O. Colmant C, et al. Among authors: druart l. Prenat Diagn. 2009 Sep;29(9):908-10. doi: 10.1002/pd.2306. Prenat Diagn. 2009. PMID: 19530104 No abstract available.

2

Tetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformations.

Haddad V, Aboura A, Tosca L, Guediche N, Mas AE, L'Herminé AC, Druart L, Picone O, Brisset S, Tachdjian G. Haddad V, et al. Among authors: druart l, l hermine ac. Am J Med Genet A. 2012 Apr;158A(4):894-900. doi: 10.1002/ajmg.a.35258. Epub 2012 Mar 14. Am J Med Genet A. 2012. PMID: 22419357

3

Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization.

Cacheux V, Tachdjian G, Druart L, Oury JF, Sérero S, Blot P, Nessmann C. Cacheux V, et al. Among authors: druart l. Prenat Diagn. 1994 Feb;14(2):79-86. doi: 10.1002/pd.1970140202. Prenat Diagn. 1994. PMID: 8183853

4

Genotype-phenotype correlation in 13q13.3-q21.3 deletion.

Tosca L, Brisset S, Petit FM, Metay C, Latour S, Lautier B, Lebas A, Druart L, Picone O, Mas AE, Prévot S, Tardieu M, Goossens M, Tachdjian G. Tosca L, et al. Among authors: druart l. Eur J Med Genet. 2011 Sep-Oct;54(5):e489-94. doi: 10.1016/j.ejmg.2011.06.004. Epub 2011 Jun 21. Eur J Med Genet. 2011. PMID: 21741501

5

Prenatal diagnosis of a (X;X) translocation by fluorescence in situ hybridization and laser scanning image cytometry.

Tachdjian G, Cacheux V, Kiefer H, Druart L, Lapierre JM, Oury JF, Blot P, Metezeau P. Tachdjian G, et al. Among authors: druart l. Fetal Diagn Ther. 1995 Nov-Dec;10(6):387-92. doi: 10.1159/000264263. Fetal Diagn Ther. 1995. PMID: 8579777

6

Unbalanced karyotype due to adjacent 1 segregation of t(11;22)(q23.3;q13.2).

Tachdjian G, Muti C, Gaudelus J, Druart L, Martin B, Tamboise E, Nessmann C. Tachdjian G, et al. Among authors: druart l. Ann Genet. 1992;35(4):231-3. Ann Genet. 1992. PMID: 1296521

7

Detection of 47,XYY trophoblast fetal cells in maternal blood by fluorescence in situ hybridization after using immunomagnetic lymphocyte depletion and flow cytometry sorting.

Cacheux V, Milesi-Fluet C, Tachdjian G, Druart L, Bruch JF, Hsi BL, Uzan S, Nessmann C. Cacheux V, et al. Among authors: druart l. Fetal Diagn Ther. 1992;7(3-4):190-4. doi: 10.1159/000263699. Fetal Diagn Ther. 1992. PMID: 1492908

8

A simple method for prenatal diagnosis of trisomy 21 on uncultured amniocytes.

Romana SP, Tachdjian G, Druart L, Cohen D, Berger R, Chérif D. Romana SP, et al. Among authors: druart l. Eur J Hum Genet. 1993;1(3):245-51. doi: 10.1159/000472418. Eur J Hum Genet. 1993. PMID: 8044650

9

Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12.

Cacheux V, Martasek P, Fougerousse F, Delfau MH, Druart L, Tachdjian G, Grandchamp B. Cacheux V, et al. Among authors: druart l. Hum Genet. 1994 Nov;94(5):557-9. doi: 10.1007/BF00211026. Hum Genet. 1994. PMID: 7959694

10

Prenatal forehead edema in 4p- deletion: the 'Greek warrior helmet' profile revisited.

Levaillant JM, Touboul C, Sinico M, Vergnaud A, Serero S, Druart L, Blondeau JR, Abd Alsamad I, Haddad B, Gérard-Blanluet M. Levaillant JM, et al. Among authors: druart l. Prenat Diagn. 2005 Dec;25(12):1150-5. doi: 10.1002/pd.1246. Prenat Diagn. 2005. PMID: 16258951 Review.

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