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Year | Number of Results |
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2015 | 2 |
2021 | 3 |
2022 | 2 |
2024 | 0 |
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A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case report.
Clin Neurol Neurosurg. 2022 Jan;212:107039. doi: 10.1016/j.clineuro.2021.107039. Epub 2021 Nov 20.
Clin Neurol Neurosurg. 2022.
PMID: 34839152
A rare cause of primary amenorrhea: LHCGR gene mutations.
Aktar Karakaya A, Çayır A, Unal E, Beştaş A, Ece Solmaz A, Kenan Haspolat Y.
Aktar Karakaya A, et al. Among authors: ece solmaz a.
Eur J Obstet Gynecol Reprod Biol. 2022 May;272:193-197. doi: 10.1016/j.ejogrb.2022.03.033. Epub 2022 Mar 19.
Eur J Obstet Gynecol Reprod Biol. 2022.
PMID: 35366614
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Clinical Contribution of Next-Generation Sequencing Multigene Panel Testing for BRCA Negative High-Risk Patients With Breast Cancer.
Ece Solmaz A, Yeniay L, Gökmen E, Zekioğlu O, Haydaroğlu A, Bilgen I, Özkınay F, Onay H.
Ece Solmaz A, et al.
Clin Breast Cancer. 2021 Dec;21(6):e647-e653. doi: 10.1016/j.clbc.2021.04.002. Epub 2021 Apr 12.
Clin Breast Cancer. 2021.
PMID: 33980423
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Mutation spectrum of the NF1 gene and genotype-phenotype correlations in Turkish patients: Seventeen novel pathogenic variants.
Ece Solmaz A, Isik E, Atik T, Ozkinay F, Onay H.
Ece Solmaz A, et al.
Clin Neurol Neurosurg. 2021 Sep;208:106884. doi: 10.1016/j.clineuro.2021.106884. Epub 2021 Aug 12.
Clin Neurol Neurosurg. 2021.
PMID: 34418705
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Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation.
Ozkinay F, Onay H, Karaca E, Arslan E, Erturk B, Ece Solmaz A, Tekin IM, Cogulu O, Aydinok Y, Vergin C.
Ozkinay F, et al. Among authors: ece solmaz a.
Hemoglobin. 2015;39(4):230-4. doi: 10.3109/03630269.2015.1038354. Epub 2015 Jun 15.
Hemoglobin. 2015.
PMID: 26076395
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Targeted multi-gene panel testing for the diagnosis of Bardet Biedl syndrome: Identification of nine novel mutations across BBS1, BBS2, BBS4, BBS7, BBS9, BBS10 genes.
Ece Solmaz A, Onay H, Atik T, Aykut A, Cerrah Gunes M, Ozalp Yuregir O, Bas VN, Hazan F, Kirbiyik O, Ozkinay F.
Ece Solmaz A, et al.
Eur J Med Genet. 2015 Dec;58(12):689-94. doi: 10.1016/j.ejmg.2015.10.011. Epub 2015 Oct 27.
Eur J Med Genet. 2015.
PMID: 26518167
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