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Author/Creator Armstrong, Linlea

21. Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel–Feil and Treacher Collins syndromes. (27th October 2014)

Authors:
Giampietro, Philip F.; Armstrong, Linlea; Stoddard, Alex; Blank, Robert D.; Livingston, Janet; Raggio, Cathy L.; Rasmussen, Kristen; Pickart, Michael; Lorier, Rachel; Turner, Amy; Sund, Sarah; Sobrera, Nara; Neptune, Enid; Sweetser, David; Santiago‐Cornier, Alberto; Broeckel, Ulrich
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 1(2015:Jan.)
Page Start:
95
Record Type:
Journal Article
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