Dundar M - Search Results

1

Unbalanced 3;22 translocation with 22q11 and 3p deletion syndrome.

Dundar M, Kiraz A, Tasdemir S, Akalin H, Kurtoglu S, Hafo F, Cine N, Savli H. Dundar M, et al. Am J Med Genet A. 2010 Nov;152A(11):2791-5. doi: 10.1002/ajmg.a.33249. Am J Med Genet A. 2010. PMID: 20949503

2

Polycystic kidney disease, biliary dysgenesis in a patient with Larsen's syndrome.

Kurtoglu S, Dundar M, Hallaç IK, Uzüm K, Okumuş Y, Oktem T. Kurtoglu S, et al. Among authors: dundar m. Clin Genet. 1997 Jun;51(6):408-11. doi: 10.1111/j.1399-0004.1997.tb02500.x. Clin Genet. 1997. PMID: 9237505

3

Patient with Weismann-Netter and Stuhl (toxopachyosteosis) syndrome with communicant hydrocephalus and arachnoid cyst.

Kurtoglu S, Dundar M, Kumandas S, Gndüz Z, Uzüm K, Durak AC, Caksen H. Kurtoglu S, et al. Among authors: dundar m. J Pediatr Endocrinol Metab. 2000 Feb;13(2):211-5. doi: 10.1515/jpem.2000.13.2.211. J Pediatr Endocrinol Metab. 2000. PMID: 10711669

4

A case with Waardenburg syndrome presenting with two separate translocations--one reciprocal and one complex.

Dundar M, Lowther G, Colgan J, Ozkul Y, Candemir Z, Saatci C, Kurtoglu S, Watt J, Morrison N. Dundar M, et al. Clin Dysmorphol. 2001 Jan;10(1):65-6. doi: 10.1097/00019605-200101000-00014. Clin Dysmorphol. 2001. PMID: 11152152

5

A novel acropectoral syndrome maps to chromosome 7q36.

Dundar M, Gordon TM, Ozyazgan I, Oguzkaya F, Ozkul Y, Cooke A, Wilkinson AG, Holloway S, Goodman FR, Tolmie JL. Dundar M, et al. J Med Genet. 2001 May;38(5):304-9. doi: 10.1136/jmg.38.5.304. J Med Genet. 2001. PMID: 11333865 Free PMC article.

6

A case of ambiguous genitalia presenting with a 45,X/46,Xr(Y)(p11.2;q11.23)/47,X,idic(Y)(p11.2),idic(Y)(p11.2) karyotype.

Dundar M, Lowther G, Acar H, Kurtoglu S, Demiryilmaz F, Kucukaydin M. Dundar M, et al. Ann Genet. 2001 Jan-Mar;44(1):5-8. doi: 10.1016/s0003-3995(00)01034-0. Ann Genet. 2001. PMID: 11334610

7

A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype.

Ozkul Y, Atabek ME, Dundar M, Kurtoglu S, Saatci C. Ozkul Y, et al. Among authors: dundar m. Ann Genet. 2002 Oct-Dec;45(4):181-3. doi: 10.1016/s0003-3995(02)01139-5. Ann Genet. 2002. PMID: 12668164

8

Associated anomalies in asymmetric crying facies and 22q11 deletion.

Akcakus M, Ozkul Y, Gunes T, Kurtoglu S, Cetin N, Kisaarslan AP, Dundar M. Akcakus M, et al. Among authors: dundar m. Genet Couns. 2003;14(3):325-30. Genet Couns. 2003. PMID: 14577677

9

Prenatal diagnosis of a fetus with partial trisomy 7p.

Ozgun MT, Batukan C, Basbug M, Akgun H, Caglayan O, Dundar M. Ozgun MT, et al. Among authors: dundar m. Fetal Diagn Ther. 2007;22(3):229-32. doi: 10.1159/000098724. Epub 2007 Jan 17. Fetal Diagn Ther. 2007. PMID: 17228165

10

Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2).

Caglayan AO, Koklu E, Saatci C, Gunes T, Ozkul Y, Narin N, Baykan A, Dundar M, Buyukkayhan D. Caglayan AO, et al. Among authors: dundar m. Ann Saudi Med. 2008 May-Jun;28(3):209-12. doi: 10.5144/0256-4947.2008.209. Ann Saudi Med. 2008. PMID: 18500176 Free PMC article. No abstract available.

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