Mail C - Search Results

1

Prenatal diagnosis and molecular cytogenetic characterization of partial dup (18p)/del (18q) due to a maternal pericentric inversion 18 in a foetus with multiple anomalies.

Atli EI, Atli E, Inan C, Varol GF, Mail C, Erbilen EA, Yalcintepe S, Demir S, Gurkan H. Atli EI, et al. Among authors: mail c. Taiwan J Obstet Gynecol. 2022 May;61(3):504-509. doi: 10.1016/j.tjog.2022.03.018. Taiwan J Obstet Gynecol. 2022. PMID: 35595446 Free article.

2

De Novo Subtelomeric 6p25.3 Deletion with Duplication of 6q23.3-q27: Genotype-Phenotype Correlation.

Atli EI, Gurkan H, Atli E, Vatansever U, Acunas B, Mail C. Atli EI, et al. Among authors: mail c. J Pediatr Genet. 2020 Mar;9(1):32-39. doi: 10.1055/s-0039-1694703. Epub 2019 Aug 12. J Pediatr Genet. 2020. PMID: 31976141 Free PMC article.

3

Concepts of Double Hit and Triple Hit Disease in Multiple Myeloma, Entity and Prognostic Significance.

Baysal M, Demirci U, Umit E, Kirkizlar HO, Atli EI, Gurkan H, Gulsaran SK, Bas V, Mail C, Demir AM. Baysal M, et al. Among authors: mail c. Sci Rep. 2020 Apr 6;10(1):5991. doi: 10.1038/s41598-020-62885-0. Sci Rep. 2020. PMID: 32249811 Free PMC article.

4

A Pilot Study of Identification Genetic Background of Craniosynostosis Cases.

Atli EI, Yalcintepe S, Atli E, Demir S, Mail C, Eker D, Kalkan R, Gurkan H. Atli EI, et al. Among authors: mail c. J Craniofac Surg. 2021 May 1;32(3):1059-1062. doi: 10.1097/SCS.0000000000007285. J Craniofac Surg. 2021. PMID: 33252532

5

The Importance of Targeted Next-Generation Sequencing Usage in Cytogenetically Normal Myeloid Malignancies.

Atli EI, Gurkan H, Atli E, Kirkizlar HO, Yalcintepe S, Demir S, Demirci U, Eker D, Mail C, Kalkan R, Demir AM. Atli EI, et al. Among authors: mail c. Mediterr J Hematol Infect Dis. 2021 Jan 1;13(1):e2021013. doi: 10.4084/MJHID.2021.013. eCollection 2021. Mediterr J Hematol Infect Dis. 2021. PMID: 33489052 Free PMC article.

6

Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes.

Yalçintepe S, Görker I, Demir S, Atli Eİ, Atli E, Tozkir H, Süt N, Özen Y, Eker D, Mail Ç, Güler HS, Zhuri D, Gurkan H. Yalçintepe S, et al. Among authors: mail c. Noro Psikiyatr Ars. 2021 Aug 26;58(3):171-175. doi: 10.29399/npa.27407. eCollection 2021. Noro Psikiyatr Ars. 2021. PMID: 34526837 Free PMC article.

7

Clinical Features of Aberrations Chromosome 22q: A Pilot Study.

Atli EI, Atli E, Yalcintepe S, Demir S, Mail C, Eker D, Ozen Y, Gurkan H. Atli EI, et al. Among authors: mail c. Glob Med Genet. 2021 Nov 9;9(1):42-50. doi: 10.1055/s-0041-1739496. eCollection 2022 Mar. Glob Med Genet. 2021. PMID: 35169783 Free PMC article.

8

Clinical Implications of Chromosome 16 Copy Number Variation.

Atli EI, Yalcintepe S, Atli E, Demir S, Mail C, Gurkan H. Atli EI, et al. Among authors: mail c. Mol Syndromol. 2022 May;13(3):184-192. doi: 10.1159/000517762. Epub 2021 Dec 15. Mol Syndromol. 2022. PMID: 35707588 Free PMC article.

9

First Report of Jacobsen Syndrome with Dextrocardia Diagnosed with del(11)(q24q25).

Yalcintepe S, Zhuri D, Sezginer Guler H, Atli E, Demir S, Atli EI, Mail C, Gurkan H. Yalcintepe S, et al. Among authors: mail c. Mol Syndromol. 2022 May;13(3):235-239. doi: 10.1159/000519149. Epub 2022 Feb 1. Mol Syndromol. 2022. PMID: 35707598 Free PMC article.

10

The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method.

Yalcintepe S, Karal Y, Demir S, Atli EI, Atli E, Eker D, Mail C, Zhuri D, Guler HS, Gurkan H. Yalcintepe S, et al. Among authors: mail c. Glob Med Genet. 2023 Jun 16;10(2):117-122. doi: 10.1055/s-0043-1770055. eCollection 2023 Jun. Glob Med Genet. 2023. PMID: 37332684 Free PMC article.

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