Tariverdian G - Search Results

1

Unique occurrence of Brachmann-de Lange syndrome in a fetus whose mother presented with a diffuse large B-cell lymphoma.

Schiffer C, Schiesser M, Lehr J, Tariverdian G, Glaeser D, Gabriel H, Mikuz G, Sergi C. Schiffer C, et al. Among authors: tariverdian g. Pathol Oncol Res. 2007;13(3):255-9. doi: 10.1007/BF02893507. Epub 2007 Oct 7. Pathol Oncol Res. 2007. PMID: 17922056 Free article. Review.

2

Agnathia-otocephaly complex: report of three cases with involvement of two different Carnegie stages.

Schiffer C, Tariverdian G, Schiesser M, Thomas MC, Sergi C. Schiffer C, et al. Among authors: tariverdian g. Am J Med Genet. 2002 Oct 1;112(2):203-8. doi: 10.1002/ajmg.10672. Am J Med Genet. 2002. PMID: 12244557

3

Wolf-Hirschhorn syndrome: case report and review of the chromosomal aberrations associated with diaphragmatic defects.

Sergi C, Schulze BR, Hager HD, Beedgen B, Zilow E, Linderkamp O, Otto HF, Tariverdian G. Sergi C, et al. Among authors: tariverdian g. Pathologica. 1998 Jun;90(3):285-93. Pathologica. 1998. PMID: 9774859 Review.

4

Short-rib-polydactyly syndrome type Verma-Naumoff-Le Marec in a fetus with histological hallmarks of type Saldino-Noonan but lacking internal organ abnormalities.

Hentze S, Sergi C, Troeger J, Revell PA, Otto HF, Tariverdian G. Hentze S, et al. Among authors: tariverdian g. Am J Med Genet. 1998 Nov 16;80(3):281-5. Am J Med Genet. 1998. PMID: 9843054

5

Ellis-van Creveld syndrome: a generalized dysplasia of enchondral ossification.

Sergi C, Voigtländer T, Zoubaa S, Hentze S, Meyberg-Solomeyer G, Troeger J, Tariverdian G, Otto HF, Schiesser M. Sergi C, et al. Among authors: tariverdian g. Pediatr Radiol. 2001 Apr;31(4):289-93. doi: 10.1007/s002470000421. Pediatr Radiol. 2001. PMID: 11321750

6

Multicolor chromosomal bar coding characterizes a de novo interstitial deletion (5)(q33.3q35.2) in a child with multiple congenital malformations.

Schiffer C, Popp S, Moshir S, Rupprath G, Düngfelder E, Hager HD, Tariverdian G, Jauch A. Schiffer C, et al. Among authors: tariverdian g. Clin Dysmorphol. 2003 Apr;12(2):129-31. doi: 10.1097/00019605-200304000-00011. Clin Dysmorphol. 2003. PMID: 12868477

7

Trisomy 8q and partial trisomy 22 in a 43-year-old man with moderate intellectual disability, epilepsy and large cell non-Hodgkin lymphoma.

Helbig I, Wirtenberger M, Jauch A, Hager HD, Tariverdian G, Hemminki K, Burwinkel B, Klaes R. Helbig I, et al. Among authors: tariverdian g. Am J Med Genet A. 2006 Aug 1;140(15):1658-62. doi: 10.1002/ajmg.a.31350. Am J Med Genet A. 2006. PMID: 16838305

8

Symptomatic heterozygosity in the Ellis-van Creveld syndrome?

Spranger S, Tariverdian G. Spranger S, et al. Among authors: tariverdian g. Clin Genet. 1995 Apr;47(4):217-20. doi: 10.1111/j.1399-0004.1995.tb03963.x. Clin Genet. 1995. PMID: 7628126

9

Rare dental abnormalities seen in oculo-facio-cardio-dental (OFCD) syndrome: three new cases and review of nine patients.

Schulze BR, Horn D, Kobelt A, Tariverdian G, Stellzig A. Schulze BR, et al. Among authors: tariverdian g. Am J Med Genet. 1999 Feb 19;82(5):429-35. doi: 10.1002/(sici)1096-8628(19990219)82:5<429::aid-ajmg13>3.0.co;2-s. Am J Med Genet. 1999. PMID: 10069716 Review.

10

Survival up to age 10 years in a patient with partial duplication 6q: case report and review of the literature.

Seel C, Hager HD, Jauch A, Tariverdian G, Zschocke J. Seel C, et al. Among authors: tariverdian g. Clin Dysmorphol. 2005 Jan;14(1):51-54. Clin Dysmorphol. 2005. PMID: 15602097

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