Berker Karaüzüm S - Search Results

1

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: berker karauzum s. Genet Couns. 2005;16(3):257-68. Genet Couns. 2005. PMID: 16259323

2

Cytogenetic findings in thirty lung carcinoma patients.

Berker-Karaüzüm S, Lüleci G, Ozbilim G, Erdoğan A, Kuzucu A, Demircan A. Berker-Karaüzüm S, et al. Cancer Genet Cytogenet. 1998 Jan 15;100(2):114-23. doi: 10.1016/s0165-4608(96)00422-0. Cancer Genet Cytogenet. 1998. PMID: 9428354

3

Telomere-specific fluorescence in situ hybridization analysis of couples with five or more recurrent miscarriages.

Yakut S, Berker-Karaüzüm S, Simşek M, Zorlu G, Trak B, Lüleci G. Yakut S, et al. Among authors: berker karauzum s. Clin Genet. 2002 Jan;61(1):26-31. doi: 10.1034/j.1399-0004.2002.610105.x. Clin Genet. 2002. PMID: 11903351

4

AZF microdeletions on the Y chromosome of infertile men from Turkey.

Sargin CF, Berker-Karaüzüm S, Manguoğlu E, Erdoğru T, Karaveli S, Gülkesen KH, Baykara M, Lüleci G. Sargin CF, et al. Among authors: berker karauzum s. Ann Genet. 2004 Jan-Mar;47(1):61-8. doi: 10.1016/j.anngen.2003.09.002. Ann Genet. 2004. PMID: 15050875

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: berker karauzum s. Genet Couns. 2005;16(2):155-9. Genet Couns. 2005. PMID: 16080295

6

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: berker karauzum s. Turk J Pediatr. 2009 Sep-Oct;51(5):453-9. Turk J Pediatr. 2009. PMID: 20112600

7

Array comparative genomic hybridization analysis of adult acute leukemia patients.

Yasar D, Karadogan I, Alanoglu G, Akkaya B, Luleci G, Salim O, Timuragaoglu A, Toruner GA, Berker-Karauzum S. Yasar D, et al. Among authors: berker karauzum s. Cancer Genet Cytogenet. 2010 Mar;197(2):122-9. doi: 10.1016/j.cancergencyto.2009.11.018. Cancer Genet Cytogenet. 2010. PMID: 20193845

8

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: berker karauzum s. Genet Couns. 2011;22(1):63-8. Genet Couns. 2011. PMID: 21614990

9

Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism.

Cetin Z, Parlak M, Altiok Clark O, Karaguzel G, Luleci G, Bircan I, Berker-Karauzum S. Cetin Z, et al. Among authors: berker karauzum s. Eur J Pediatr. 2013 Sep;172(9):1215-9. doi: 10.1007/s00431-013-2028-1. Epub 2013 May 8. Eur J Pediatr. 2013. PMID: 23652939

10

Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1).

Cetin Z, Mendilcioglu I, Yakut S, Berker-Karauzum S, Karaman B, Luleci G. Cetin Z, et al. Among authors: berker karauzum s. Balkan J Med Genet. 2011 Jun;14(1):57-60. doi: 10.2478/v10034-011-0019-y. Balkan J Med Genet. 2011. PMID: 24052704 Free PMC article.

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