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Human Molecular Genetics|August 22, 2002
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotypeTim Cundy, Madhuri Hegde, Dorit Naot, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|March 20, 2009
Guideline for resuscitation in cardiac arrest after cardiac surgeryJoel Dunning, Alessandro Fabbri, Philippe H Kolh, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 19, 2018
Mutations That Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta PhenotypeTim Cundy, Michael Dray, John Delahunt, et al.
European Journal of Human Genetics : EJHG|October 23, 2003
The deleted in colorectal carcinoma (DCC) gene 201 R --> G polymorphism: no evidence for genetic association with autoimmune diseaseRichard J Hall, Marilyn E Merriman, Rachel A Green, et al.
Nature Genetics|May 31, 2011
Genome-wide association identifies three new susceptibility loci for Paget's disease of boneOmar M E Albagha, Sachin E Wani, Micaela R Visconti, et al.
The New Zealand Medical Journal|February 17, 2017
Proposed new industry code on unhealthy food marketing to children and young people: will it make a difference?Boyd Swinburn, Stefanie Vandevijvere, Alistair Woodward, et al.
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