Mihçi E - Search Results

1

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. Turk J Pediatr. 2009 Sep-Oct;51(5):510-4. Turk J Pediatr. 2009. PMID: 20112612

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

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

7

Unilateral pulmonary agenesis associated with colloidal goiter in a newborn: a case report.

Gökhan GA, Ozbilim G, Bozova S, Güra A, Ongun H, Mihci E, Arslan G. Gökhan GA, et al. Among authors: mihci e. Turk J Pediatr. 2005 Jul-Sep;47(3):295-7. Turk J Pediatr. 2005. PMID: 16250321

8

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

9

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

10

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

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