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Targeted resequencing identifies
PTCH1
as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network
Supplemental Material
Files in this Data Supplement:
Supp Table 1.xlsx
Supp Table 8.xlsx
Supp Tables 2-7.docx
Supplemental Figures.doc
Supplemental Note.doc
Supplemental Table Legends.docx
This Article
Published in Advance
February 18, 2016
, doi:
10.1101/gr.196048.115
Genome Res.
April 2016
vol. 26
no. 4
474-485
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