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RT @DDG2P: ASXL3; Possible DD Gene; 13757; Bohring-Opitz Like syndrome ; Monoallelic; Loss of function; http://t.co/TKu5V7TATk
RT @DDG2P: ASXL3; Possible DD Gene; 13757; Bohring-Opitz Like syndrome ; Monoallelic; Loss of function; http://t.co/TKu5V7TATk
RT @GholsonLyon: De novo truncating muts in ASXL3 are associated w novel clinical phenotype w similarities to Bohring-Opitz syndrome. http:…
RT @GenomeMedicine: From sequencing to identifying a syndrome: Hilger Ropers, Richard Gibbs & team find syndrome similar to Bohring-Opitz h…
A highlight on http://t.co/DIHOAPRlq3 discusses what we're learning about syndromes similar to Bohring-Optiz http://t.co/Xd07Zu4KLe.