Mihçi E - Search Results

1

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: mihci e. Genet Couns. 2005;16(2):155-9. Genet Couns. 2005. PMID: 16080295

2

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

Mihçi E, Taçoy S, Haspolat S, Karaali K. Mihçi E, et al. 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

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. Fetal Diagn Ther. 2005 May-Jun;20(3):167-70. doi: 10.1159/000083898. Fetal Diagn Ther. 2005. PMID: 15824491

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: mihci e. Indian J Med Sci. 2005 Apr;59(4):150-5. Indian J Med Sci. 2005. PMID: 15876779

5

Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.

Caliskan MO, Karauzum SB, Mihci E, Tacoy S, Luleci G. Caliskan MO, et al. Among authors: mihci e. Genet Couns. 2005;16(2):129-38. Genet Couns. 2005. PMID: 16080292

6

M-FISH applications in clinical genetics.

Cetin Z, Berker Karaüzüm S, Yakut S, Mihçi E, Baumer A, Wey E, Taçoy S, Bağci G, Lüleci G. Cetin Z, et al. Among authors: mihci e. Genet Couns. 2005;16(3):257-68. Genet Couns. 2005. PMID: 16259323

7

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: mihci e. J Dermatol. 2006 Mar;33(3):219-22. doi: 10.1111/j.1346-8138.2006.00050.x. J Dermatol. 2006. PMID: 16620231

8

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. Turk J Pediatr. 2007 Jul-Sep;49(3):322-6. Turk J Pediatr. 2007. PMID: 17990591

9

Oral-facial digital syndrome type 1.

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

10

Neutrophil oxidative metabolism in Down syndrome patients with congenital heart defects.

Akinci O, Mihci E, Tacoy S, Kardelen F, Keser I, Aslan M. Akinci O, et al. Among authors: mihci e. Environ Mol Mutagen. 2010 Jan;51(1):57-63. doi: 10.1002/em.20511. Environ Mol Mutagen. 2010. PMID: 19593803

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