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Seminars in Cell & Developmental Biology|February 25, 2016
Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxyAnna R Duncan, Mustafa K KhokhaBrain Research|September 30, 2009
Ontogeny and the effects of exogenous and endogenous glucocorticoids on tight junction protein expression in ovine cerebral corticesAnna R Duncan, Grazyna B Sadowska, Barbara S StonestreetDevelopmental Biology|August 10, 2019
Alkylglycerol monooxygenase, a heterotaxy candidate gene, regulates left-right patterning via Wnt signalingAnna R Duncan, Delfina P González, Florencia Del Viso, et al.Developmental Cell|January 2, 2018
RAPGEF5 Regulates Nuclear Translocation of β-CateninJohn N Griffin, Florencia Del Viso, Anna R Duncan, et al.BMC Medical Genetics|June 29, 2011
Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNESteven E Boyden, Anna R Duncan, Elicia A Estrella, et al.Muscle & Nerve|March 3, 2016
Homozygous nonsense mutation in SGCA is a common cause of limb-girdle muscular dystrophy in Assiut, EgyptHemakumar M Reddy, Sherifa A Hamed, Monkol Lek, et al.Neurogenetics|July 13, 2010
Efficient identification of novel mutations in patients with limb girdle muscular dystrophySteven E Boyden, Mustafa A Salih, Anna R Duncan, et al.Journal of Perinatology : Official Journal of the California Perinatal Association|December 9, 2020
COVID-19: neonatal-perinatal perspectivesAlejandra Barrero-Castillero, Kristyn S Beam, Laura B Bernardini, et al.Neurogenetics|February 29, 2012
Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicoresSteven E Boyden, Lane J Mahoney, Genri Kawahara, et al.Human Molecular Genetics|October 19, 2020
De novo variants in MPP5 cause global developmental delay and behavioral changesNoelle Sterling, Anna R Duncan, Raehee Park, et al.Pageof 2