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- 2025
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Mark
Polygenic scores in Familial breast cancer cases with and without pathogenic variants and the risk of contralateral breast cancer
- Contribution to journal › Article
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Mark
Validation of Guidelines for Genetic Investigation of Myeloid Neoplasms with Germline Predisposition : Results from a Prospective Cohort Study
- Contribution to journal › Article
- 2024
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Mark
The clinical spectrum of ataxia telangiectasia in a cohort in Sweden
- Contribution to journal › Article
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Mark
How to manage patients with germline DDX41 variants : Recommendations from the Nordic working group on germline predisposition for myeloid neoplasms
- Contribution to journal › Article
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Mark
Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis
- Contribution to journal › Article
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Mark
Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors—a nationwide, prospective Swedish study
- Contribution to journal › Article
- 2023
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Mark
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer
- Contribution to journal › Article
- 2017
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Mark
Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS and neurological symptoms
- Contribution to journal › Article
- 2016
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Mark
Successful Hematopoietic Stem Cell Transplantation in a Patient with LPS-Responsive Beige-Like Anchor (LRBA) Gene Mutation
- Contribution to journal › Article
