Oğur G - Search Results

1

657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family.

Tekin M, Doğu F, Taçyíldiz N, Akar E, Ikincioğullari A, Oğur G, Yavuz G, Babacan E, Akar N. Tekin M, et al. Among authors: ogur g. Clin Genet. 2002 Jul;62(1):84-8. doi: 10.1034/j.1399-0004.2002.620112.x. Clin Genet. 2002. PMID: 12123493

2

The acrocallosal syndrome in a Turkish boy.

Yüksel M, Caliskan M, Oğur G, Ozmen M, Dolunay G, Apak S. Yüksel M, et al. Among authors: ogur g. J Med Genet. 1990 Jan;27(1):48-9. doi: 10.1136/jmg.27.1.48. J Med Genet. 1990. PMID: 2308155 Free PMC article.

3

Clinical, ultrastructural and biochemical studies in two sibs with Ehlers-Danlos syndrome type VI-B-like features.

Oğur G, Baykan N, De Paepe A, Steinmann B, Quatacker J, Kuseyrí F, Yüksel-Apak M. Oğur G, et al. Clin Genet. 1994 Dec;46(6):417-22. doi: 10.1111/j.1399-0004.1994.tb04409.x. Clin Genet. 1994. PMID: 7889658

4

del(17)(q25) in a patient with hairy cell leukemia: a new clonal chromosome abnormality.

Sucak GT, Ogur G, Topal G, Ataoglu O, Cankus G, Haznedar R. Sucak GT, et al. Among authors: ogur g. Cancer Genet Cytogenet. 1998 Jan 15;100(2):152-4. doi: 10.1016/s0165-4608(97)00026-5. Cancer Genet Cytogenet. 1998. PMID: 9428360

5

Yağci M, Sucak GT, Oğur G, Haznedar R. Yağci M, et al. Among authors: ogur g. Cancer Genet Cytogenet. 2001 Aug;129(1):43-6. doi: 10.1016/s0165-4608(01)00423-x. Cancer Genet Cytogenet. 2001. PMID: 11520565

6

Clinical and cytogenetic studies of two cases of Klinefelter syndrome with hereditary retinoblastoma and rhabdomyosarcoma.

Oğur G, Sengun Z, Arel-Kiliç G, De Busscher C, Başaran S, Ozbek U, Ayan I, Sariban E, Vamos E. Oğur G, et al. Cancer Genet Cytogenet. 1996 Jul 1;89(1):77-81. doi: 10.1016/0165-4608(96)00352-4. Cancer Genet Cytogenet. 1996. PMID: 8689618

7

Vesicourethral reflux-induced renal failure in a patient with ICF syndrome due to a novel DNMT3B mutation.

Kutluğ S, Ogur G, Yilmaz A, Thijssen PE, Abur U, Yildiran A. Kutluğ S, et al. Among authors: ogur g. Am J Med Genet A. 2016 Dec;170(12):3253-3257. doi: 10.1002/ajmg.a.37866. Epub 2016 Sep 8. Am J Med Genet A. 2016. PMID: 27604394

8

Syndrome of congenital cutis laxa with ligamentous laxity and delayed development: report of a brother and sister from Turkey.

Oğur G, Yüksel-Apak M, Demiryont M. Oğur G, et al. Am J Med Genet. 1990 Sep;37(1):6-9. doi: 10.1002/ajmg.1320370103. Am J Med Genet. 1990. PMID: 1700609

9

Association of syndactyly, ectodermal dysplasia, and cleft lip and palate: report of two sibs from Turkey.

Oğur G, Yüksel M. Oğur G, et al. J Med Genet. 1988 Jan;25(1):37-40. J Med Genet. 1988. PMID: 2832607 Free PMC article. Review.

10

Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.

Okten G, Sezer O, Günes S, Küçüködük S, Oğur G. Okten G, et al. Among authors: ogur g. Genet Couns. 2009;20(4):341-7. Genet Couns. 2009. PMID: 20162869

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