Tachdjian G - Search Results

1

Prenatal diagnosis of Crigler-Najjar syndrome type I by single-strand conformation polymorphism (SSCP).

Francoual J, Trioche P, Mokrani C, Seboui H, Khrouf N, Chalas J, Clement M, Capel L, Tachdjian G, Labrune P. Francoual J, et al. Among authors: tachdjian g. Prenat Diagn. 2002 Oct;22(10):914-6. doi: 10.1002/pd.443. Prenat Diagn. 2002. PMID: 12378576

2

Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study.

Lapierre JM, Cacheux V, Luton D, Collot N, Oury JF, Aurias A, Tachdjian G. Lapierre JM, et al. Among authors: tachdjian g. Prenat Diagn. 2000 Feb;20(2):123-31. doi: 10.1002/(sici)1097-0223(200002)20:2<123::aid-pd762>3.0.co;2-b. Prenat Diagn. 2000. PMID: 10694684

3

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

4

Discordant prenatal diagnosis of trisomy 21 due to mosaic structural rearrangements of chromosome 21.

Brisset S, Aboura A, Audibert F, Costa JM, L'Herminé AC, Gautier V, Frydman R, Tachdjian G. Brisset S, et al. Among authors: tachdjian g. Prenat Diagn. 2003 Jun;23(6):461-9. doi: 10.1002/pd.620. Prenat Diagn. 2003. PMID: 12813759

5

Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15.

L'Herminé AC, Aboura A, Brisset S, Cuisset L, Castaigne V, Labrune P, Frydman R, Tachdjian G. L'Herminé AC, et al. Among authors: tachdjian g. Prenat Diagn. 2003 Nov;23(11):938-43. doi: 10.1002/pd.732. Prenat Diagn. 2003. PMID: 14634983

6

Double-outlet right ventricle with absent left ventricle and mitral atresia in a fetus with a deletion 22q12.

L'herminé-Coulomb A, Houyel L, Aboura A, Audibert F, Dal Soglio D, Tachdjian G. L'herminé-Coulomb A, et al. Among authors: tachdjian g. Prenat Diagn. 2004 Sep;24(9):708-12. doi: 10.1002/pd.970. Prenat Diagn. 2004. PMID: 15386448

7

De novo interstitial direct duplication of Xq21.1q25 associated with skewed X-inactivation pattern.

Tachdjian G, Aboura A, Benkhalifa M, Creveaux I, Foix-Hélias L, Gadisseux JF, Boespflug-Tanguy O, Mohammed M, Labrune P. Tachdjian G, et al. Am J Med Genet A. 2004 Dec 15;131(3):273-80. doi: 10.1002/ajmg.a.30359. Am J Med Genet A. 2004. PMID: 15526291

8

Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndrome.

Petit FM, Gajdos V, Parisot F, Capel L, Aboura A, Lachaux A, Tachdjian G, Poüs C, Labrune P. Petit FM, et al. Among authors: tachdjian g. Eur J Hum Genet. 2005 Mar;13(3):278-82. doi: 10.1038/sj.ejhg.5201342. Eur J Hum Genet. 2005. PMID: 15586176

9

De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.

Brisset S, Kasakyan S, L'Herminé AC, Mairovitz V, Gautier E, Aubry MC, Benkhalifa M, Tachdjian G. Brisset S, et al. Among authors: tachdjian g. Prenat Diagn. 2006 Mar;26(3):206-13. doi: 10.1002/pd.1379. Prenat Diagn. 2006. PMID: 16450348

10

Early and rapid prenatal diagnosis of monosomy 2q36.1 in trophoblast cells.

Tachdjian G, Aboura A, Brisset S, Dommergues M, Gajdos V, Labrune P. Tachdjian G, et al. Fetal Diagn Ther. 2006;21(5):428-32. doi: 10.1159/000093885. Fetal Diagn Ther. 2006. PMID: 16912492

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