Associated Papers
Osteomesopyknosis associated with a novel ALOX5 variant that impacts the RANKL pathway.
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Supplement: MGG3-12-e2471-s001.xls › Sheet1
Identification of NCAN as a candidate gene for developmental dyslexia.
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Supplement: 41598_2017_10175_MOESM3_ESM.xls › 3935-rare_exonic_variants
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