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Journal for Healthcare Quality : Official Publication of the National Association for Healthcare Quality|June 5, 2015
Routinization of HIV Testing in an Inpatient Setting: A Systematic Process for Organizational ChangeJamie L Mignano, Lucy Miner, Christina Cafeo, et al.Public Health Research (Southampton, England)|May 31, 2023
Impact of a social prescribing intervention in North East England on adults with type 2 diabetes: the SPRING_NE multimethod studySuzanne Moffatt, John Wildman, Tessa M Pollard, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 27, 2023
GNA11 Variants Identified in Patients with Hypercalcemia or HypocalcemiaSarah A Howles, Caroline M Gorvin, Treena Cranston, et al.European Journal of Human Genetics : EJHG|May 28, 2009
Novel SOX2 partner-factor domain mutation in a four-generation familyMarija Mihelec, Peter Abraham, Kate Gibson, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2012
Next-generation sequencing in health-care delivery: lessons from the functional analysis of rhodopsinWayne I L Davies, Susan M Downes, Josephine K Fu, et al.Molecular Genetics & Genomic Medicine|October 23, 2018
Penetrance and expressivity of the R858H CACNA1C variant in a five-generation pedigree segregating an arrhythmogenic channelopathyR J McKinlay Gardner, Ian G Crozier, Alex L Binfield, et al.European Journal of Human Genetics : EJHG|October 16, 2008
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndromeThomas E Neumann, Judith Allanson, Ines Kavamura, et al.Nature Genetics|November 28, 2018
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regionsPatricia Heyn, Clare V Logan, Adeline Fluteau, et al.Nature Genetics|December 5, 2006
Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndromeMarco Tartaglia, Len A Pennacchio, Chen Zhao, et al.American Journal of Medical Genetics. Part A|September 27, 2016
Clinical and genetic aspects of KBG syndromeKaren Low, Tazeen Ashraf, Natalie Canham, et al.Pageof 7