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Your search keyword '"Lindstrand, Anna"' showing total 6 results

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2. Different mutations in PDE4D associated with developmental disorders with mirror phenotypes

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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