Tachdjian G - Search Results

1

Terminal 14q32.33 deletion: genotype-phenotype correlation.

Maurin ML, Brisset S, Le Lorc'h M, Poncet V, Trioche P, Aboura A, Labrune P, Tachdjian G. Maurin ML, et al. Among authors: tachdjian g. Am J Med Genet A. 2006 Nov 1;140(21):2324-9. doi: 10.1002/ajmg.a.31438. Am J Med Genet A. 2006. PMID: 17022077 Review.

2

Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH).

Benzacken B, Lapierre JM, Siffroi JP, Chalvon A, Tachdjian G. Benzacken B, et al. Among authors: tachdjian g. Clin Genet. 1998 Oct;54(4):334-40. doi: 10.1034/j.1399-0004.1998.5440412.x. Clin Genet. 1998. PMID: 9831346

3

De novo inverted duplication 9p21pter involving telomeric repeated sequences.

Sanlaville D, Baumann C, Lapierre JM, Romana S, Collot N, Cacheux V, Turleau C, Tachdjian G. Sanlaville D, et al. Among authors: tachdjian g. Am J Med Genet. 1999 Mar 12;83(2):125-31. doi: 10.1002/(sici)1096-8628(19990312)83:2<125::aid-ajmg8>3.0.co;2-0. Am J Med Genet. 1999. PMID: 10190483 Review.

4

Cytogenetic analysis from DNA by comparative genomic hybridization.

Tachdjian G, Aboura A, Lapierre JM, Viguié F. Tachdjian G, et al. Ann Genet. 2000 Jul-Dec;43(3-4):147-54. doi: 10.1016/s0003-3995(00)01028-5. Ann Genet. 2000. PMID: 11164197 Review.

5

Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomalies.

Tabet AC, Aboura A, Dauge MC, Audibert F, Coulomb A, Batallan A, Couturier-Turpin MH, Feldmann G, Tachdjian G. Tabet AC, et al. Among authors: tachdjian g. Prenat Diagn. 2001 Aug;21(8):613-8. doi: 10.1002/pd.115. Prenat Diagn. 2001. PMID: 11536256

6

Assisting reproduction of infertile men carrying a Robertsonian translocation.

Frydman N, Romana S, Le Lorc'h M, Vekemans M, Frydman R, Tachdjian G. Frydman N, et al. Among authors: tachdjian g. Hum Reprod. 2001 Nov;16(11):2274-7. doi: 10.1093/humrep/16.11.2274. Hum Reprod. 2001. PMID: 11679503

7

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

8

Molecular cytogenetic analysis of a Xp21.3-pter deletion in a family with normal and short stature.

Tachdjian G, Perreaux F, Aboura A, Chevalier P, Portnoi MF, Esteva B, Trioche P, Labrune P. Tachdjian G, et al. Clin Genet. 2002 Feb;61(2):163-5. doi: 10.1034/j.1399-0004.2002.610214.x. Clin Genet. 2002. PMID: 11940094 No abstract available.

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

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

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