Cinbis M[au] - Search Results

Year	Number of Results
1992	1
1993	2
2001	1
2002	1
2003	1
2004	1
2006	1
2007	1
2009	2
2010	1
2012	1
2024	0

1

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

2

Neonatal goiter caused by expectorant usage.

Bostanci I, Sarioģlu A, Ergin H, Akşit A, Cinbiş M, Akalin N. Bostanci I, et al. Among authors: cinbis m. J Pediatr Endocrinol Metab. 2001 Sep-Oct;14(8):1161-2. doi: 10.1515/jpem-2001-0815. J Pediatr Endocrinol Metab. 2001. PMID: 11592576

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

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

5

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

6

The role of RELN in lissencephaly and neuropsychiatric disease.

Chang BS, Duzcan F, Kim S, Cinbis M, Aggarwal A, Apse KA, Ozdel O, Atmaca M, Zencir S, Bagci H, Walsh CA. Chang BS, et al. Among authors: cinbis m. Am J Med Genet B Neuropsychiatr Genet. 2007 Jan 5;144B(1):58-63. doi: 10.1002/ajmg.b.30392. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 16958033

7

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.

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

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

10

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

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