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- 2024
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Mark
The psychosocial impact of prostate cancer screening for BRCA1 and BRCA2 carriers
(
- Contribution to journal › Article
- 2023
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Mark
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
(
- Contribution to journal › Article
-
Mark
European Association of Urology Guidelines on Upper Urinary Tract Urothelial Carcinoma : 2023 Update
(
- Contribution to journal › Scientific review
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Mark
Treatment and long-term outcome in primary nephrogenic diabetes insipidus
(
- Contribution to journal › Article
- 2022
-
Mark
Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle-aged and older adults: A population-based cohort study
(
- Contribution to journal › Letter
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Mark
2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension
(
- Contribution to journal › Article
- 2021
-
Mark
Genetic Screening in Patients Suspected of Inherited Bleeding Disorders
2021) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
- 2017
-
Mark
Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations
(
- Contribution to journal › Article
- 2016
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Mark
'It made you think twice' - an interview study of women's perception of a web-based decision aid concerning screening and diagnostic testing for fetal anomalies
(
- Contribution to journal › Article
- 2015
-
Mark
Risk Screening, Testing, and Diagnosis : Ethical Aspects
2015) p.698-705(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2014
-
Mark
Neuroacanthocytosis - Clinical variability (a report on six cases)
2014) Eighteenth International Congress of Parkinson's Disease and Movement Disorders In Movement Disorders 29(Suppl 1). p.194-194(
- Contribution to journal › Published meeting abstract
- 2008
-
Mark
EuroGentest: DNA-based testing for heritable disorders in Europe
(
- Contribution to journal › Article
- 2007
-
Mark
Malignant hyperthermia and central core disease causative mutations in Swedish patients.
(
- Contribution to journal › Article
- 2004
-
Mark
BRCA1 och BRCA2 har nått kliniken. Tioårigt fynd av genmutation ger nu möjlighet förebygga ärftlig bröstcan
(
- Contribution to journal › Article
- 2002
-
Mark
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
(
- Contribution to journal › Article
- 1999
-
Mark
Long-term psychological effects of carrier testing and prenatal diagnosis of haemophilia: Comparison with a control group
(
- Contribution to journal › Article