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Seminars in Arthritis and Rheumatism|November 16, 2013
Epigenetics and methylation in the rheumatic diseasesFlore Zufferey, Frances M K Williams, Tim D SpectorAmerican Journal of Medical Genetics. Part A|May 31, 2013
Acro-osteolysis, keloid like-lesions, distinctive facial features, and overgrowth: two newly recognized patients with premature aging syndrome, Penttinen typeFlore Zufferey, Smaïl Hadj-Rabia, Annachiara De Sandre-Giovannoli, et al.Genome Medicine|September 5, 2018
Increased DNA methylation variability in rheumatoid arthritis-discordant monozygotic twinsAmy P Webster, Darren Plant, Simone Ecker, et al.American Journal of Medical Genetics. Part A|June 9, 2012
Recurrent mutations in the CDKL5 gene: genotype-phenotype relationshipsNadia Bahi-Buisson, Nathalie Villeneuve, Emilie Caietta, et al.Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|May 17, 2011
16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridization in persistent pulmonary hypertension of the newbornFlore Zufferey, Danielle Martinet, Maria-Chiara Osterheld, et al.Plos One|April 5, 2013
Rare genomic structural variants in complex disease: lessons from the replication of associations with obesityRobin G Walters, Lachlan J M Coin, Aimo Ruokonen, et al.Journal of Medical Genetics|October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersFlore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.Nature|September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locusSébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.Pageof 1