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Journal of Psychiatric Research|December 6, 2000
Impaired eye expression recognition in schizophreniaJ M Kington, L A Jones, A A Watt, et al.Journal of Continuing Education in Nursing|October 16, 2004
Development of a web-based genetics institute for a nursing audienceCynthia A Prows, Carol Hetteberg, Robert J Hopkin, et al.Annals of Human Genetics|November 3, 2023
Phenotypic variability in Joubert syndrome is partially explained by ciliary pathophysiologyJoshua W Owens, Robert J Hopkin, Lisa J Martin, et al.Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 15, 2001
Case of complex craniofacial anomalies, bilateral nasal proboscides, palatal pituitary, upper limbs reduction, and amnion rupture sequence: disorganization phenotype?J Stanek, G de Courten-Myers, A G Spaulding, et al.Neuromuscular Disorders : NMD|March 21, 2001
Cardiac abnormalities and skeletal muscle weakness in carriers of Duchenne and Becker muscular dystrophies and controlsL Grain, M Cortina-Borja, C Forfar, et al.American Journal of Medical Genetics. Part A|April 23, 2003
Long-term survival in a patient with del(18)(q12.2q21.1)Brad T Tinkle, Carol A Christianson, Elizabeth K Schorry, et al.Pediatric Radiology|August 7, 2019
Prenatal evaluation of the Sakoda complexUsha D Nagaraj, Rohitha Moudgal, Robert J Hopkin, et al.Journal of Perinatology : Official Journal of the California Perinatal Association|June 20, 2019
Fetal brain MRI findings and neonatal outcome of common diagnosis at a tertiary care centerMonica S Arroyo, Robert J Hopkin, Usha D Nagaraj, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 17, 2007
Genetic service providers' practices and attitudes regarding adolescent genetic testing for carrier statusTrisha J Multhaupt-Buell, Anne Lovell, Lisa Mills, et al.The Biochemical Journal|May 15, 1994
Surfactant protein D binding to alveolar macrophagesK Miyamura, L E Leigh, J Lu, et al.Pageof 20