Lüleci G - 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: luleci g. Genet Couns. 2005;16(2):155-9. Genet Couns. 2005. PMID: 16080295

2

Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.

Cetin Z, Mihci E, Keser I, Karaali K, Berker S, Luleci G. Cetin Z, et al. Among authors: luleci g. Genet Couns. 2012;23(2):239-47. Genet Couns. 2012. PMID: 22876583

3

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: luleci g. Genet Couns. 2005;16(2):129-38. Genet Couns. 2005. PMID: 16080292

4

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: luleci g. Genet Couns. 2005;16(3):257-68. Genet Couns. 2005. PMID: 16259323

5

De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome.

Yakut S, Cetin Z, Berker-Karauzum S, Mihci E, Mendilcioglu I, Luleci G. Yakut S, et al. Among authors: luleci g. Genet Couns. 2011;22(1):63-8. Genet Couns. 2011. PMID: 21614990

6

Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13).

Cetin Z, Mihci E, Keser I, Luleci G. Cetin Z, et al. Among authors: luleci g. Genet Couns. 2012;23(2):207-14. Genet Couns. 2012. PMID: 22876579

7

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

8

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: luleci g. Turk J Pediatr. 2009 Sep-Oct;51(5):453-9. Turk J Pediatr. 2009. PMID: 20112600

9

Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12.

Cetin Z, Mihci E, Yakut S, Keser I, Karauzum SB, Luleci G. Cetin Z, et al. Among authors: luleci g. Am J Med Genet A. 2011 Feb;155A(2):349-52. doi: 10.1002/ajmg.a.33811. Epub 2011 Jan 13. Am J Med Genet A. 2011. PMID: 21271652

10

A patient with Down syndrome with a de novo derivative chromosome 21.

Cetin Z, Yakut S, Mihci E, Manguoglu AE, Berker S, Keser I, Luleci G. Cetin Z, et al. Among authors: luleci g. Gene. 2012 Oct 10;507(2):159-64. doi: 10.1016/j.gene.2012.07.018. Epub 2012 Jul 22. Gene. 2012. PMID: 22827956

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