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Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families.
- Published in:
- Blood Transfusion (17232007), 2018, v. 16, n. 1, p. 105, doi. 10.2450/2016.0098-16
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- Article
Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p.M771I, p.L881R and p.P1413L.
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- Blood Transfusion (17232007), 2017, v. 15, n. 6, p. 548, doi. 10.2450/2016.0034-16
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- Article
Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p.Cys398Tyr mutation.
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- Blood Transfusion (17232007), 2014, v. 12, n. 3, p. 446, doi. 10.2450/2014.0022-14
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- Article
Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p.Cys398Tyr mutation.
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- Cumhuriyet Medical Journal, 2018, v. 40, n. 3, p. 315, doi. 10.7197/223.vi.439869
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- Article
Exploring the role of miRNAs in the diagnosis of MODY3.
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- Turkish Journal of Medical Sciences, 2018, v. 48, n. 3, p. 620, doi. 10.3906/sag-1711-98
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- Article
Gene therapy in haemophilia: literature review and regional perspectives for Turkey.
- Published in:
- Therapeutic Advances in Hematology, 2022, v. 13, p. 1, doi. 10.1177/20406207221104591
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- Article
Higher Expression of the Novel Gene Upregulated Gene 4 in Two Acute Lymphoblastic Leukemia Patients with Poor Prednisolone Response.
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- Acta Haematologica, 2012, v. 128, n. 2, p. 73, doi. 10.1159/000338220
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- Publication type:
- Article
Higher Expression of the Novel Gene Upregulated Gene 4 in Two Acute Lymphoblastic Leukemia Patients with Poor Prednisolone Response.
- Published in:
- Acta Haematologica, 2012, v. 128, n. 2, p. 73, doi. 10.1159/000338220
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- Publication type:
- Article
The Molecular Genetics of von Willebrand Disease.
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- Turkish Journal of Hematology, 2012, v. 29, n. 4, p. 313, doi. 10.5505/tjh.2012.39205
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- Article
A Common VWF Exon 28 Haplotype in the Turkish Population.
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- Clinical & Applied Thrombosis/Hemostasis, 2013, v. 19, n. 5, p. 550, doi. 10.1177/1076029612441054
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- Article
Molecular Characterization of FXI Deficiency.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2011, v. 17, n. 1, p. 27, doi. 10.1177/1076029609355587
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- Article