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Author/Creator Cox, Gerald F.

1. Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome. Issue 1 (24th October 2020)

Authors:
Dyment, David A.; O'Donnell‐Luria, Anne; Agrawal, Pankaj B.; Coban Akdemir, Zeynep; Aleck, Kyrieckos A.; Antaki, Danny; Al Sharhan, Hind; Au, Ping‐Yee B.; Aydin, Hatip; Beggs, Alan H.; Bilguvar, Kaya; Boerwinkle, Eric; Brand, Harrison; Brownstein, Catherine A.; Buyske, Steve; Chodirker, Bernard; ...
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 1(2021)
Page Start:
119
Record Type:
Journal Article
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4. Differences in Presentation and Outcomes Between Children With Familial Dilated Cardiomyopathy and Children With Idiopathic Dilated Cardiomyopathy: A Report From the Pediatric Cardiomyopathy Registry Study Group. (February 2017)

Authors:
Rusconi, Paolo; Wilkinson, James D.; Sleeper, Lynn A.; Lu, Minmin; Cox, Gerald F.; Towbin, Jeffrey A.; Colan, Steven D.; Webber, Steven A.; Canter, Charles E.; Ware, Stephanie M.; Hsu, Daphne T.; Chung, Wendy K.; Jefferies, John L.; Cordero, Christina; Lipshultz, Steven E.
Journal:
Circulation
Issue:
Volume 10:Number 2(2017)
Page Start:
Record Type:
Journal Article
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5. Novel Mutations Widen the Phenotypic Spectrum of Slow Skeletal/β‐Cardiac Myosin (MYH7) Distal Myopathy. Issue 7 (21st May 2014)

Authors:
Lamont, Phillipa J.; Wallefeld, William; Hilton‐Jones, David; Udd, Bjarne; Argov, Zohar; Barboi, Alexandru C.; Bonneman, Carsten; Boycott, Kym M.; Bushby, Kate; Connolly, Anne M.; Davies, Nicholas; Beggs, Alan H.; Cox, Gerald F.; Dastgir, Jahannaz; DeChene, Elizabeth T.; Gooding, Rebecca; Jungblu...
Journal:
Human mutation
Issue:
Volume 35:Issue 7(2014:Jul.)
Page Start:
868
Record Type:
Journal Article
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