Altiok Clark O - Search Results

1

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: altiok clark o. Gene. 2022 May 20;823:146322. doi: 10.1016/j.gene.2022.146322. Epub 2022 Feb 25. Gene. 2022. PMID: 35219815

2

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: altiok clark o. 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

3

Mosaic Intrachromosomal Triplication of (12)(p11.2p13) in a Patient with Pallister-Killian Syndrome.

Yakut S, Mihci E, Altiok Clark O, Cetin Z, Keser I, Berker S, Luleci G. Yakut S, et al. Among authors: altiok clark o. Balkan J Med Genet. 2012 Jun;15(1):61-4. doi: 10.2478/v10034-012-0010-2. Balkan J Med Genet. 2012. PMID: 24052725 Free PMC article.

4

The association of Klinefelter syndrome and multiple pterygium syndrome: an unusual presentation.

Nur BG, Altıok-Clark O, Toylu A, Lüleci G, Mıhçı E. Nur BG, et al. Among authors: altiok clark o. Turk J Pediatr. 2013 Sep-Oct;55(5):559-63. Turk J Pediatr. 2013. PMID: 24382544

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: altiok clark o. Andrologia. 2015 Feb;47(1):112-5. doi: 10.1111/and.12232. Epub 2014 Jan 28. Andrologia. 2015. PMID: 24471893

6

Bilateral congenital cataracts in an infant with Klinefelter syndrome.

Nur BG, Altıok-Clark Ö, İlhan HD, Sayar E, Yücel İ, Mıhçı E. Nur BG, et al. Among authors: altiok clark o. Turk J Pediatr. 2014 Sep-Oct;56(5):546-50. Turk J Pediatr. 2014. PMID: 26022594

7

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: altiok clark o. Genet Couns. 2016;27(1):51-66. Genet Couns. 2016. PMID: 27192892

8

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: altiok clark o. Cytogenet Genome Res. 2021;161(3-4):153-159. doi: 10.1159/000515368. Epub 2021 Jul 6. Cytogenet Genome Res. 2021. PMID: 34229322

9

Investigation of the relationship between reproductive disorders and chromosomal abnormalities in a large-scale, single-center 10-year retrospective study.

Ertosun MG, Araci DG, Peker A, Uzuner SY, Toylu A, Ozekinci M, Usta MF, Altiok Clark O. Ertosun MG, et al. Among authors: altiok clark o. J Gynecol Obstet Hum Reprod. 2022 Nov;51(9):102467. doi: 10.1016/j.jogoh.2022.102467. Epub 2022 Aug 28. J Gynecol Obstet Hum Reprod. 2022. PMID: 36044979

10

A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism Due to a Novel Homozygous Variant in the SCNN1B Gene.

Singin B, Donbaloğlu Z, Barsal Çetiner E, Çetin K, Özkan Zarif N, Çelik K, Mıhçı E, Altıok Clark Ö, Tuhan H, Parlak M. Singin B, et al. Among authors: altiok clark o. J Clin Res Pediatr Endocrinol. 2024 Dec 26. doi: 10.4274/jcrpe.galenos.2024.2024-10-5. Online ahead of print. J Clin Res Pediatr Endocrinol. 2024. PMID: 39723761 Free article.

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