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The American Journal of Gastroenterology|August 10, 2005
Prospective multicenter study of eligibility for antiviral therapy among 4,084 U.S. veterans with chronic hepatitis C virus infectionEdmund J Bini, Norbert Bräu, Sue Currie, et al.Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|July 18, 2021
FACE-Q Craniofacial Module: Part 1 validation of CLEFT-Q scales for use in children and young adults with facial conditionsAnne F Klassen, Charlene Rae, Karen Wy Wong Riff, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2020
Correction: SMAD6 variants in craniosynostosis: genotype and phenotype evaluationEduardo Calpena, Araceli Cuellar, Krithi Bala, et al.Brain : a Journal of Neurology|February 27, 2019
Randomized trial of intermittent intraputamenal glial cell line-derived neurotrophic factor in Parkinson's diseaseAlan Whone, Matthias Luz, Mihaela Boca, et al.BMJ Open|October 11, 2020
'A sword of Damocles': patient and caregiver beliefs, attitudes and perspectives on presymptomatic testing for autosomal dominant polycystic kidney disease: a focus group studyCharlotte Logeman, Yeoungjee Cho, Benedicte Sautenet, et al.Cancer Research|February 12, 2005
Genetic linkage of prostate cancer risk to the chromosome 3 region bearing FHITGarry P Larson, Yan Ding, Li S-C Cheng, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2020
SMAD6 variants in craniosynostosis: genotype and phenotype evaluationEduardo Calpena, Araceli Cuellar, Krithi Bala, et al.Journal of Parkinson'S Disease|March 5, 2019
Extended Treatment with Glial Cell Line-Derived Neurotrophic Factor in Parkinson's DiseaseAlan L Whone, Mihaela Boca, Matthias Luz, et al.Nature Genetics|January 29, 2013
Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesisStephen R F Twigg, Elena Vorgia, Simon J McGowan, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2023
Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetranceRebecca S Tooze, Kerry A Miller, Sigrid M A Swagemakers, et al.Pageof 69