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Clinical Genetics|May 14, 2011
The new Ghent criteria for Marfan syndrome: what do they change?L Faivre, G Collod-Beroud, L Adès, et al.Nature Communications|December 2, 2025
Artificial intelligence for quantum computingYuri Alexeev, Marwa H Farag, Taylor L Patti, et al.Journal of Burn Care & Research : Official Publication of the American Burn Association|October 11, 2007
American Burn Association consensus conference to define sepsis and infection in burnsDavid G Greenhalgh, Jeffrey R Saffle, James H Holmes, et al.Molecular Psychiatry|April 5, 2017
A paternal methyl donor-rich diet altered cognitive and neural functions in offspring miceD P Ryan, K S Henzel, B L Pearson, et al.Journal of Burn Care & Research : Official Publication of the American Burn Association|March 29, 2006
Effects of oxandrolone on outcome measures in the severely burned: a multicenter prospective randomized double-blind trialSteven E Wolf, Linda S Edelman, Nathan Kemalyan, et al.Nature Genetics|August 10, 2000
Genome-wide, large-scale production of mutant mice by ENU mutagenesisM H Hrabé de Angelis, H Flaswinkel, H Fuchs, et al.Human Mutation|December 21, 2012
Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein armsDinu Antony, Anita Becker-Heck, Maimoona A Zariwala, et al.Nature Medicine|January 29, 2020
Somatic gene editing ameliorates skeletal and cardiac muscle failure in pig and human models of Duchenne muscular dystrophyA Moretti, L Fonteyne, F Giesert, et al.American Journal of Respiratory and Critical Care Medicine|February 27, 2014
Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotypeMichael R Knowles, Lawrence E Ostrowski, Margaret W Leigh, et al.American Journal of Human Genetics|September 24, 2013
Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein armsMichael R Knowles, Lawrence E Ostrowski, Niki T Loges, et al.Pageof 188