Division of Clinical Genetics
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- 2023
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Mark
The complexity of kidney disease and diagnosing it - Cystatin C, selective glomerular hypofiltration syndromes and proteome regulation
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- Contribution to journal › Scientific review
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Mark
Inactivation of RB1, CDKN2A and TP53 have distinct effects on genomic stability at side-by-side comparison in karyotypically normal cells
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- Contribution to journal › Article
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Mark
Updated Stroke Gene Panels : Rapid evolution of knowledge on monogenic causes of stroke
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- Contribution to journal › Article
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Mark
UROSCAN and UROSCANSEQ : a large-scale multicenter effort towards translation of molecular bladder cancer subtypes into clinical practice–from biobank to RNA-sequencing in real time
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- Contribution to journal › Article
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Mark
Insertion of the CXXC domain of KMT2A into YAP1 : An unusual mechanism behind the formation of a chimeric oncogenic protein
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- Contribution to journal › Article
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Mark
Impact of 1q gains on treatment outcomes of patients with newly diagnosed multiple myeloma in a real-world Swedish population receiving modern treatment
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- Contribution to journal › Article
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Mark
A Swedish SCA34 family with late onset ataxia, cerebellar atrophy and ocular movement abnormalities with a novel mutation in ELOVL4
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- Contribution to journal › Published meeting abstract
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Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer
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- Contribution to journal › Article
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Mark
Functional In Vivo Screening Identifies microRNAs Regulating Metastatic Dissemination of Prostate Cancer Cells to Bone Marrow
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- Contribution to journal › Article
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Mark
The sarcopenia index measured using the lumbar paraspinal muscle is associated with prognosis in endometrial cancer
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- Contribution to journal › Article