Tachdjian G - 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: tachdjian g. Prenat Diagn. 2009 Sep;29(9):908-10. doi: 10.1002/pd.2306. Prenat Diagn. 2009. PMID: 19530104 No abstract available.

2

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. Ann Genet. 1992;35(4):231-3. Ann Genet. 1992. PMID: 1296521

3

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: tachdjian g. Fetal Diagn Ther. 1992;7(3-4):190-4. doi: 10.1159/000263699. Fetal Diagn Ther. 1992. PMID: 1492908

4

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: tachdjian g. Hum Genet. 1994 Nov;94(5):557-9. doi: 10.1007/BF00211026. Hum Genet. 1994. PMID: 7959694

5

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: tachdjian g. Eur J Hum Genet. 1993;1(3):245-51. doi: 10.1159/000472418. Eur J Hum Genet. 1993. PMID: 8044650

6

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: tachdjian g. Prenat Diagn. 1994 Feb;14(2):79-86. doi: 10.1002/pd.1970140202. Prenat Diagn. 1994. PMID: 8183853

7

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. Fetal Diagn Ther. 1995 Nov-Dec;10(6):387-92. doi: 10.1159/000264263. Fetal Diagn Ther. 1995. PMID: 8579777

8

De novo interstitial direct duplication 1(q23.1q31.1) in a fetus with Pierre Robin sequence and camptodactyly.

Aboura A, Coulomb-L'Herminé A, Audibert F, Capron F, Frydman R, Tachdjian G. Aboura A, et al. Among authors: tachdjian g. Am J Med Genet. 2002 Mar 1;108(2):153-9. doi: 10.1002/ajmg.10219. Am J Med Genet. 2002. PMID: 11857566

9

Female pseudohermaphroditism in a fetus with a deletion 9(q22.2q31.1).

L'Herminé AC, Aboura A, Simon-Bouy B, Robin F, Audibert F, Strouk N, Capron F, Frydman R, Tachdjian G. L'Herminé AC, et al. Among authors: tachdjian g. Prenat Diagn. 2002 Aug;22(8):652-5. doi: 10.1002/pd.353. Prenat Diagn. 2002. PMID: 12210571

10

Deletion in the ABL gene resulting from a meiotic recombination of a maternal (3;22;9)(q22;q12;q34.1) translocation.

Aboura A, Labrune P, Perreaux F, Poncet V, Brisset S, Foix-L'Helias L, Tachdjian G. Aboura A, et al. Among authors: tachdjian g. J Med Genet. 2003 Jan;40(1):e6. doi: 10.1136/jmg.40.1.e6. J Med Genet. 2003. PMID: 12525554 Free PMC article. No abstract available.

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