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CCR3.255
CCR3.255
http://dx.doi.org/10.1002/CCR3.255
A 6q14.1-q15 microdeletion in a male patient with severe autistic disorder, lack of oral language, and dysmorphic features with concomitant presence of a maternally inherited Xp22.31 copy number gain.
P356
Q41135371-498217A4-AFF6-4961-B987-B9F7F8784243
P356
CCR3.255
http://dx.doi.org/10.1002/CCR3.255