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        - 2024
- 
                        Mark
        Development of the Parent-to-Infant Bonding Scale : Validation in Swedish Mothers and Fathers in Community and Clinical Contexts
    (2024) In Child Psychiatry and Human Development- Contribution to journal › Article
 
- 2022
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                        Mark
        Targeting elevated heme levels to treat a mouse model for Diamond-Blackfan Anemia
    
    - Contribution to journal › Article
 
- 2020
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                        Mark
        Genome-wide association meta-analysis of single-nucleotide polymorphisms and symptomatic venous thromboembolism during therapy for acute lymphoblastic leukemia and lymphoma in caucasian children
    
    - Contribution to journal › Article
 
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                        Mark
        Parenting stress and its correlates in an infant mental health unit : a cross-sectional study
    
    - Contribution to journal › Article
 
- 2018
- 
                        Mark
        Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7
    
    - Contribution to journal › Article
 
- 
                        Mark
        Establishing a regional paediatric registry improved the overview and detection of side effects in children on anticoagulants
    
    - Contribution to journal › Article
 
- 
                        Mark
        SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies
    
    - Contribution to journal › Article
 
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                        Mark
        Thromboembolism in acute lymphoblastic leukemia : Results of nopho all2008 protocol treatment in patients aged 1 to 45 years
    
    - Contribution to journal › Article
 
- 
                        Mark
        Macrolide resistant pertussis in an infant whose mother was not vaccinated against pertussis
    (2018) ESPID 1028: 36th Annual Meeting of the European Society for Paediatric Infectious Diseases- Contribution to conference › Abstract
 
- 2017
- 
                        Mark
        Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS and neurological symptoms
    
    - Contribution to journal › Article
 
