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211 results

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Page 1
Waardenburg anophthalmia syndrome: report and review.
Cogulu O, Ozkinay F, Gündüz C, Sapmaz G, Ozkinay C. Cogulu O, et al. Among authors: gunduz c. Am J Med Genet. 2000 Jan 17;90(2):173-4. Am J Med Genet. 2000. PMID: 10607960 Review. No abstract available.
Multiple pterygium syndrome.
Ozkinay FF, Ozkinay C, Akin H, Azarsiz S, Gündüz C. Ozkinay FF, et al. Among authors: gunduz c. Indian J Pediatr. 1997 Jan-Feb;64(1):113-6. doi: 10.1007/BF02795791. Indian J Pediatr. 1997. PMID: 10771823
Cerebro-costo-mandibular syndrome: a case report.
Ozkinay F, Cogulu O, Gündüz C, Cankaya T, Ozkinay C. Ozkinay F, et al. Among authors: gunduz c. Pediatr Int. 2001 Oct;43(5):522-4. doi: 10.1046/j.1442-200x.2001.01430.x. Pediatr Int. 2001. PMID: 11737720 No abstract available.
The second case with 47, XY, + 8 [38] / 45, X0.
Coğulu O, Tirpan C, Ozkinay F, Gündüz C, Ozkinay C. Coğulu O, et al. Among authors: gunduz c. Turk J Pediatr. 2002 Jan-Mar;44(1):86-9. Turk J Pediatr. 2002. PMID: 11858390 No abstract available.
New chromosome rearrangement in acute lymphoblastic leukemia.
Gündüz C, Coğulu O, Cetingül N, Kantar M, Cankaya T, Ozkinay C, Ozkinay F. Gündüz C, et al. Cancer Genet Cytogenet. 2002 Sep;137(2):150-2. doi: 10.1016/s0165-4608(02)00561-7. Cancer Genet Cytogenet. 2002. PMID: 12393288
Prenatal detection of a pure trisomy 10p case.
Gunduz C, Cogulu O, Sagol S, Zekioglu O, Ozkinay C, Ozkinay F. Gunduz C, et al. Prenat Diagn. 2003 Apr;23(4):356-8. doi: 10.1002/pd.591. Prenat Diagn. 2003. PMID: 12673647 No abstract available.
Mandibuloacral dysplasia with absent breast development.
Cogulu O, Gunduz C, Arkun R, Darcan S, Kadioglu B, Ozkinay F, Ozkinay C. Cogulu O, et al. Among authors: gunduz c. Am J Med Genet A. 2003 Jun 15;119A(3):391-2. doi: 10.1002/ajmg.a.10169. Am J Med Genet A. 2003. PMID: 12784312 No abstract available.
211 results