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

Publisher： John Wiley & Sons Inc

E-ISSN： 2050-0904|3|6|415-423

ISSN： 2050-0904

Source： Clinical Case Reports, Vol.3, Iss.6, 2015-06, pp. : 415-423

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