Berker Karauzum S - Search Results

1

Coexistence of a Homozygous Chromosome 4q35.2 Deletion and Hidden IQSEC2 Pathogenic Variant in a Child with Intellectual Disability.

Karaman Mercan T, Altiok Clark O, Erkal O, Nur B, Mihci E, Karaman B, Senol AU, Berker Karauzum S. Karaman Mercan T, et al. Among authors: berker karauzum s. Cytogenet Genome Res. 2021;161(3-4):153-159. doi: 10.1159/000515368. Epub 2021 Jul 6. Cytogenet Genome Res. 2021. PMID: 34229322

2

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

3

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

4

Evaluation of exonic copy numbers of SMN1 and SMN2 genes in SMA.

Arikan Y, Berker Karauzum S, Uysal H, Mihci E, Nur B, Duman O, Haspolat S, Altiok Clark O, Toylu A. Arikan Y, et al. Among authors: berker karauzum s. Gene. 2022 May 20;823:146322. doi: 10.1016/j.gene.2022.146322. Epub 2022 Feb 25. Gene. 2022. PMID: 35219815

5

Ring chromosome 21 and monosomy 21 mosaicism in a patient with azoospermia.

Cetin Z, Altiok-Clark O, Sevuk M, Berker Karauzum S. Cetin Z, et al. Among authors: berker karauzum s. Andrologia. 2015 Feb;47(1):112-5. doi: 10.1111/and.12232. Epub 2014 Jan 28. Andrologia. 2015. PMID: 24471893

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

7

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

8

Celiac disease in patients with Williams-Beuren syndrome.

Mıhçı E, Nur BG, Berker-Karaüzüm S, Yılmaz A, Artan R. Mıhçı E, et al. Among authors: berker karauzum s. Turk J Pediatr. 2015 Nov-Dec;57(6):599-604. Turk J Pediatr. 2015. PMID: 27735799

9

A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOMPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES.

Cetin Z, Altiok-Clark O, Yakut S, Guzel-Nur B, Mihci E, Berker-Karauzum S. Cetin Z, et al. Among authors: berker karauzum s. Genet Couns. 2016;27(1):51-66. Genet Couns. 2016. PMID: 27192892

10

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

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