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Acta Neuropathologica|November 1, 2002
Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortexAkiyoshi Kakita, Shintaro Hayashi, Francesca Moro, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 28, 2002
Doublecortin is required in mice for lamination of the hippocampus but not the neocortexJoseph C Corbo, Thomas A Deuel, Jeffrey M Long, et al.
Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|October 29, 2021
Evaluation of advanced methods and materials for construction of scintillation detector light guidesRaymond R Raylman, Matthew B Johnson, Joshua Bintrim, et al.
Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry|May 29, 2013
Layer-by-layer assembly of ferrocene-modified linear polyethylenimine redox polymer filmsJared L DeLuca, David P Hickey, Daniel A Bamper, et al.
American Journal of Medical Genetics. Part A|October 4, 2011
Phenotypic heterogeneity in Woodhouse-Sakati syndrome: two new families with a mutation in the C2orf37 geneTawfeg Ben-Omran, Rehab Ali, Mariam Almureikhi, et al.
Human Molecular Genetics|September 29, 2009
Detecting natural selection by empirical comparison to random regions of the genomeFuli Yu, Alon Keinan, Hua Chen, et al.
Neuron|January 3, 2006
Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowthThomas A S Deuel, Judy S Liu, Joseph C Corbo, et al.
Nucleic Acids Research|November 30, 2017
PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimationMaxwell A Sherman, Alison R Barton, Michael A Lodato, et al.
Briefings in Bioinformatics|September 29, 2016
Rare variant association test in family-based sequencing studiesXuefeng Wang, Zhenyu Zhang, Nathan Morris, et al.
American Journal of Medical Genetics. Part A|May 12, 2005
EMX2-independent familial schizencephaly: clinical and genetic analysesIan Tietjen, Füsun Erdogan, Sophie Currier, et al.
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