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Paper Details

Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder.
Hum Genet
3
2018
1p36, ASD, ASDs, MSSNG, NOC2L, SAMD11, autism spectrum disorder, autism spectrum disorders, exome variant, rare exome variants, regulatory region variant, rs185038034, rs200195897, rs566472488
Author NameAffiliation
Elizabeth E BlueUniversity of Washington
Elizabeth E BlueUniversity of Washington
Dong-Hui ChenUniversity of Washington
Wendy H RaskindUniversity of Washington
Wendy H RaskindUniversity of Washington
Wendy H RaskindUniversity of Washington
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