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. Author manuscript; available in PMC: 2019 Apr 2.
Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2018 Aug 4;177(6):589–595. doi: 10.1002/ajmg.b.32673

Fig. 1:

Fig. 1:

Pedigree of our large Chinese family with deletion at the NRXN3 locus

Black-filled symbol represents ASD affected individual, gray-filled symbols represent affected individuals, and unfilled symbols represent apparently unaffected individuals. Proband is marked with an arrow. Clinical diagnosis and segregation of the NRXN3 deletion are shown.