Found: 10
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Delineating the genetic heterogeneity of OCA in Hungarian patients.
- Published in:
- European Journal of Medical Research, 2017, v. 22, p. 1, doi. 10.1186/s40001-017-0262-0
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- Article
Landscape of BCL2 Resistance Mutations in a Real-World Cohort of Patients with Relapsed/Refractory Chronic Lymphocytic Leukemia Treated with Venetoclax.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 6, p. 5802, doi. 10.3390/ijms24065802
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- Article
Identification of two novel mutations in the SLC45A2 gene in a Hungarian pedigree affected by unusual OCA type 4.
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- BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0386-7
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- Article
High-throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosis.
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- Brain & Behavior, 2017, v. 7, n. 4, p. n/a, doi. 10.1002/brb3.669
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- Article
Nuclear Factor κB Activation in a Type V Pityriasis Rubra Pilaris Patient Harboring Multiple <italic>CARD14</italic> Variants.
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- Frontiers in Immunology, 2018, p. N.PAG, doi. 10.3389/fimmu.2018.01564
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- Article
Low‐burden TP53 mutations represent frequent genetic events in CLL with an increased risk for treatment initiation.
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- Journal of Pathology: Clinical Research, 2024, v. 10, n. 1, p. 1, doi. 10.1002/cjp2.351
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- Article
Revealing a Phenotypical Appearance of Ibrutinib Resistance in Patients With Chronic Lymphocytic Leukaemia by Flow Cytometry.
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- Pathology & Oncology Research, 2022, v. 28, p. 1, doi. 10.3389/pore.2022.1610659
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- Article
Phenotypic diversity of the recurrent p.Val379Leu missense mutation of the TGM1 gene.
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- Dermatologica Sinica, 2018, v. 36, n. 2, p. 89, doi. 10.1016/j.dsi.2017.08.001
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- Article
Phenotypical diversity of patients with LEOPARD syndrome carrying the worldwide recurrent p.Tyr279Cys PTPN11 mutation.
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- Archives of Dermatological Research, 2015, v. 307, n. 10, p. 891, doi. 10.1007/s00403-015-1597-4
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- Article
CTSC and Papillon-Lefèvre syndrome: detection of recurrent mutations in Hungarian patients, a review of published variants and database update.
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- Molecular Genetics & Genomic Medicine, 2014, v. 2, n. 3, p. 217, doi. 10.1002/mgg3.61
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- Article