6 results on '"Lindstrand, Anna"'
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2. Different mutations in PDE4D associated with developmental disorders with mirror phenotypes
3. A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT
4. Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes
5. CTNND2—a candidate gene for reading problems and mild intellectual disability
6. Different mutations inPDE4Dassociated with developmental disorders with mirror phenotypes
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