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Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A

September 14, 2010 DYRK1A

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In DYRK1A Gene Research, DYRK1A Patient Research Tags 2014 and older
← Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly Function and regulation of DYRK1A: towards understanding down syndrome →

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