Author:
Manshaei Roozbeh,Merico Daniele,Reuter Miriam S.,Engchuan Worrawat,Mojarad Bahareh A.,Chaturvedi Rajiv,Heung Tracy,Pellecchia Giovanna,Zarrei Mehdi,Nalpathamkalam Thomas,Khan Reem,Okello John B. A.,Liston Eriskay,Curtis Meredith,Yuen Ryan K. C.,Marshall Christian R.,Jobling Rebekah K.,Oechslin Erwin,Wald Rachel M.,Silversides Candice K.,Scherer Stephen W.,Kim Raymond H.,Bassett Anne S.
Funder
Garfield Weston Foundation
Canadian Institutes of Health Research
Subject
Genetics (clinical),Genetics,Molecular Medicine
Reference56 articles.
1. A method and server for predicting damaging missense mutations.;Adzhubei;Nat. Methods,2010
2. Congenital heart disease and Robinow syndrome.;Atalay;Clin. Dysmorphol.,1993
3. AKAP12 deficiency impairs VEGF-induced endothelial cell migration and sprouting.;Benz;Acta Physiol.,2019
4. Biallelic loss-of-function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome.;Birgmeier;Am. J. Med. Genet. Part A,2018
5. Sertoli cell signaling by Desert hedgehog regulates the male germline.;Bitgood;Curr. Biol.,1996