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Author/Creator Ip, Eddie

1. A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data. (March 2018)

Authors:
Szot, Justin O.; Cuny, Hartmut; Blue, Gillian M.; Humphreys, David T.; Ip, Eddie; Harrison, Katrina; Sholler, Gary F.; Giannoulatou, Eleni; Leo, Paul; Duncan, Emma L.; Sparrow, Duncan B.; Ho, Joshua W.K.; Graham, Robert M.; Pachter, Nicholas; Chapman, Gavin; Winlaw, David S.; Dunwoodie, Sally L.
Journal:
Circulation
Issue:
Volume 11:Number 3(2018)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice. (4th December 2020)

Authors:
Martin, Ella M M A; Enriquez, Annabelle; Sparrow, Duncan B; Humphreys, David T; McInerney-Leo, Aideen M; Leo, Paul J; Duncan, Emma L; Iyer, Kavitha R; Greasby, Joelene A; Ip, Eddie; Giannoulatou, Eleni; Sheng, Delicia; Wohler, Elizabeth; Dimartino, Clémantine; Amiel, Jeanne; Capri, Yline; Lehalle...
Journal:
Human molecular genetics
Issue:
Volume 29:Number 22(2020)
Page Start:
3662
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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