Tacoy S - Search Results

1

Sliding type hernia and ectopic pancreatic tissue in the stomach with renal agenesis and ear abnormalities: branchio-oto-renal syndrome or hemifacial microsomia with additional findings.

Ozkinay F, Cogulu O, Ozkinay C, Aydogdu S, Gunduz C, Tacoy S. Ozkinay F, et al. Among authors: tacoy s. Am J Med Genet A. 2003 Aug 1;120A(4):562-3. doi: 10.1002/ajmg.a.20109. Am J Med Genet A. 2003. PMID: 12884440 No abstract available.

2

Central nervous system abnormalities in Kabuki (Niikawa-Kuroki) syndrome.

Mihçi E, Taçoy S, Haspolat S, Karaali K. Mihçi E, et al. Among authors: tacoy s. Am J Med Genet. 2002 Sep 1;111(4):448-9. doi: 10.1002/ajmg.10573. Am J Med Genet. 2002. PMID: 12210310 No abstract available.

3

Oral-facial digital syndrome type 1.

Mihci E, Tacoy S, Ozbilim G, Franco B. Mihci E, et al. Among authors: tacoy s. Indian Pediatr. 2007 Nov;44(11):854-6. Indian Pediatr. 2007. PMID: 18057484 Free article.

4

Molecular analysis of fragile X syndrome in Antalya Province.

Bilgen T, Keser I, Mihci E, Haspolat S, Tacoy S, Luleci G. Bilgen T, et al. Among authors: tacoy s. Indian J Med Sci. 2005 Apr;59(4):150-5. Indian J Med Sci. 2005. PMID: 15876779

5

A case with de novo interstitial deletion of chromosome 7q21.1-q22.

Manguoğlu E, Berker-Karaüzüm S, Baumer A, Mihçi E, Taçoy S, Lüleci G, Schinzel A. Manguoğlu E, et al. Among authors: tacoy s. Genet Couns. 2005;16(2):155-9. Genet Couns. 2005. PMID: 16080295

6

Maternal origin and clinical findings in a case with trisomy 22.

Mihçi E, Taçoy S, Yakut S, Ongun H, Keser I, Kiliçarslan B, Bağci G, Lüleci G. Mihçi E, et al. Among authors: tacoy s. Turk J Pediatr. 2007 Jul-Sep;49(3):322-6. Turk J Pediatr. 2007. PMID: 17990591

7

Evaluation of a fetus with Neu-Laxova syndrome through prenatal, clinical, and pathological findings.

Mihci E, Simsek M, Mendilcioglu I, Tacoy S, Karaveli S. Mihci E, et al. Among authors: tacoy s. Fetal Diagn Ther. 2005 May-Jun;20(3):167-70. doi: 10.1159/000083898. Fetal Diagn Ther. 2005. PMID: 15824491

8

Aplasia cutis congenita: three cases with three different underlying etiologies.

Mihçi E, Erişir S, Taçoy S, Lüleci G, Alpsoy E, Oygür N. Mihçi E, et al. Among authors: tacoy s. Turk J Pediatr. 2009 Sep-Oct;51(5):510-4. Turk J Pediatr. 2009. PMID: 20112612

9

Subtelomeric rearrangements of dysmorphic children with idiopathic mental retardation reveal 8 different chromosomal anomalies.

Mihçi E, Ozcan M, Berker-Karaüzüm S, Keser I, Taçoy S, Hapsolat S, Lüleci G. Mihçi E, et al. Among authors: tacoy s. Turk J Pediatr. 2009 Sep-Oct;51(5):453-9. Turk J Pediatr. 2009. PMID: 20112600

10

PHACES syndrome presenting as hemangiomas, sternal clefting and congenital ulcerations on the helices.

Durusoy C, Mihci E, Tacoy S, Ozaydin E, Alpsoy E. Durusoy C, et al. Among authors: tacoy s. J Dermatol. 2006 Mar;33(3):219-22. doi: 10.1111/j.1346-8138.2006.00050.x. J Dermatol. 2006. PMID: 16620231

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