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MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)

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AbstractFullPdf
Nov 201812913432
Dec 201835639880
Jan 201920620326
Feb 201917016524
Mar 201917617123
Apr 201927927141
May 201918717749
Jun 201910710137
Jul 2019777722
Aug 2019535110
Sep 2019747412
Oct 2019776623
Nov 2019676118
Total19581949397