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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 14, 2012
The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): a review of clinical features, radiographic features, and WISP3 mutations in 63 affected individualsNuria Garcia Segarra, Laureane Mittaz, Ana Belinda Campos-Xavier, et al.
Research Report (Health Effects Institute)|August 23, 2003
Biomarkers in Czech workers exposed to 1,3-butadiene: a transitional epidemiologic studyRichard J Albertini, Radim J Srám, Pamela M Vacek, et al.
Human Molecular Genetics|January 31, 2015
Mosaic structural variation in children with developmental disordersDaniel A King, Wendy D Jones, Yanick J Crow, et al.
The Journal of Clinical Investigation|July 14, 2015
B56δ-related protein phosphatase 2A dysfunction identified in patients with intellectual disabilityGunnar Houge, Dorien Haesen, Lisenka E L M Vissers, et al.
Scientific Data|August 7, 2021
Biotic threats for 23 major non-native tree species in EuropeElisabeth Pötzelsberger, Martin M Gossner, Ludwig Beenken, et al.
JCO Precision Oncology|June 23, 2022
RAD51B Harbors Germline Mutations Associated With Pancreatic Ductal AdenocarcinomaFanfan Xie, Ding Ding, Cong Lin, et al.
Genome Research|October 13, 2009
The NIH Human Microbiome Project, Jane Peterson, Susan Garges, et al.
Ambio|February 25, 2026
Freshwater biodiversity in a rapidly changing Arctic: An expert horizon scan of key research questionsJoseph M Culp, Michael Power, Kirsten S Christoffersen, et al.
Science (New York, N.Y.)|November 10, 2018
Quantifying the contribution of recessive coding variation to developmental disordersHilary C Martin, Wendy D Jones, Rebecca McIntyre, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosisSonja A de Munnik, Louise S Bicknell, Salim Aftimos, et al.
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