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Genetic Characterization of Hereditary Cancer Syndromes Based on Targeted Next-Generation Sequencing.
Mol Syndromol. 2022 Feb;13(2):123-131. doi: 10.1159/000518927. Epub 2021 Nov 4.
Mol Syndromol. 2022.
PMID: 35418818
Free PMC article.
Witteveen-Kolk syndrome: The first patient from Turkey.
Ercoskun P, Yuce Kahraman C.
Ercoskun P, et al.
Am J Med Genet A. 2021 Feb;185(2):617-619. doi: 10.1002/ajmg.a.61950. Epub 2020 Nov 3.
Am J Med Genet A. 2021.
PMID: 33142042
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Novel Findings in Floating-Harbor Syndrome and a Mini-Review of the Literature.
Ercoskun P, Yuce-Kahraman C.
Ercoskun P, et al.
Mol Syndromol. 2021 Mar;12(1):52-56. doi: 10.1159/000512050. Epub 2020 Nov 30.
Mol Syndromol. 2021.
PMID: 33776628
Free PMC article.
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A new case of Turnpenny-Fry syndrome.
Ercoskun P, Yuce Kahraman C, Adanur Saglam K, Kanjee M, Tatar A.
Ercoskun P, et al.
Am J Med Genet A. 2022 Feb;188(2):688-691. doi: 10.1002/ajmg.a.62560. Epub 2021 Nov 9.
Am J Med Genet A. 2022.
PMID: 34750959
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A novel genomic variant in two siblings with very low-density lipoprotein receptor-associated cerebellar hypoplasia.
Yuce Kahraman C, Ercoskun P, Yakar O, Tatar A.
Yuce Kahraman C, et al. Among authors: ercoskun p.
Clin Dysmorphol. 2022 Apr 1;31(2):98-100. doi: 10.1097/MCD.0000000000000409.
Clin Dysmorphol. 2022.
PMID: 34954733
No abstract available.
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A Novel nonsense variant in the CDH2 gene associated with ACOGS: A case report.
Kanjee M, Yuce Kahraman C, Ercoskun P, Tatar A, Kahraman M.
Kanjee M, et al. Among authors: ercoskun p.
Am J Med Genet A. 2022 Sep;188(9):2815-2818. doi: 10.1002/ajmg.a.62861. Epub 2022 Jun 16.
Am J Med Genet A. 2022.
PMID: 35708058
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The right to terminate pregnancy (abortion): reflections from Turkey.
Şenol HKE, Ercoşkun P.
Şenol HKE, et al. Among authors: ercoskun p.
J Law Biosci. 2023 Sep 3;10(2):lsad023. doi: 10.1093/jlb/lsad023. eCollection 2023 Jul-Dec.
J Law Biosci. 2023.
PMID: 37671116
Free PMC article.
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