Cinbis M - Search Results

1

Can cytomegalovirus cause brachydactyly? A case report and review of the literature.

Cinbis M, Topcu M, Balci S. Cinbis M, et al. Clin Genet. 1993 Apr;43(4):204-6. doi: 10.1111/j.1399-0004.1993.tb04449.x. Clin Genet. 1993. PMID: 8392455

2

Intramedullary astrocytoma presenting as spinal muscular atrophy.

Aysun S, Cinbiş M, Ozcan OE. Aysun S, et al. Among authors: cinbis m. J Child Neurol. 1993 Oct;8(4):354-6. doi: 10.1177/088307389300800411. J Child Neurol. 1993. PMID: 8228031

3

Molecular genetic analyses in neurofibromatosis type 1 patients with tumors.

Oguzkan S, Terzi YK, Cinbis M, Anlar B, Aysun S, Ayter S. Oguzkan S, et al. Among authors: cinbis m. Cancer Genet Cytogenet. 2006 Mar;165(2):167-71. doi: 10.1016/j.cancergencyto.2005.08.029. Cancer Genet Cytogenet. 2006. PMID: 16527612

4

Alice in Wonderland syndrome as an initial manifestation of Epstein-Barr virus infection.

Cinbis M, Aysun S. Cinbis M, et al. Br J Ophthalmol. 1992 May;76(5):316. doi: 10.1136/bjo.76.5.316. Br J Ophthalmol. 1992. PMID: 1390519 Free PMC article.

5

Dandy-Walker's variant and tetralogy of Fallot with atrial septal defect and patent ductus arteriosus and primary hypothyroidy--a new association.

Ozdemir O, Polat A, Cinbis M, Kurt F, Kucuktasci K, Kiroglu Y. Ozdemir O, et al. Among authors: cinbis m. Indian J Pediatr. 2009 Apr;76(4):433-5. doi: 10.1007/s12098-009-0130-1. Epub 2009 May 2. Indian J Pediatr. 2009. PMID: 19412588

6

Molecular analysis of neurofibromatosis type 1 in Turkish families using polymorphic markers.

Oğuzkan S, Cinbiş M, Ayter S, Anlar B, Aysun S. Oğuzkan S, et al. Among authors: cinbis m. Turk J Pediatr. 2003 Jul-Sep;45(3):192-7. Turk J Pediatr. 2003. PMID: 14696795

7

Familial segmental neurofibromatosis.

Oguzkan S, Cinbis M, Ayter S, Anlar B, Aysun S. Oguzkan S, et al. Among authors: cinbis m. J Child Neurol. 2004 May;19(5):392-4. doi: 10.1177/088307380401900515. J Child Neurol. 2004. PMID: 15224714

8

Cognitive functions in neurofibromatosis type 1 patients and unaffected siblings.

Erdoğan-Bakar E, Cinbiş M, Ozyürek H, Kiriş N, Altunbaşak S, Anlar B. Erdoğan-Bakar E, et al. Among authors: cinbis m. Turk J Pediatr. 2009 Nov-Dec;51(6):565-71. Turk J Pediatr. 2009. PMID: 20196390

9

Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome.

Semerci CN, Cinbis M, Ullmann R, Steininger A, Bahce M, Yagci B, Ozden S, Sabir N, Gumus D, Tepeli E, Arteaga J, Mutchinick OM. Semerci CN, et al. Among authors: cinbis m. Am J Med Genet A. 2010 Jul;152A(7):1724-9. doi: 10.1002/ajmg.a.33383. Am J Med Genet A. 2010. PMID: 20578131

10

Terminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocation.

Bağcı G, Çetin GO, Semerci N, Toruner GA, Cinbiş M. Bağcı G, et al. Among authors: cinbis m. Clin Dysmorphol. 2012 Jan;21(1):37-41. doi: 10.1097/MCD.0b013e32834d6ba3. Clin Dysmorphol. 2012. PMID: 22143350

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