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American Journal of Medical Genetics. Part A|October 12, 2013
Clinical, genetic, and molecular aspects of split-hand/foot malformation: an updateFiorella Gurrieri, David B EvermanEuropean Journal of Pediatrics|May 28, 2003
Respiratory failure requiring extracorporeal membrane oxygenation after sodium phosphate enema intoxicationDavid B Everman, Mara E Nitu, Brian R JacobsExpert Opinion on Orphan Drugs|February 7, 2017
Neurobiologically-based treatments in Rett syndrome: opportunities and challengesWalter E Kaufmann, Jennifer L Stallworth, David B Everman, et al.Human Molecular Genetics|January 10, 2019
A neurodevelopmental disorder caused by mutations in the VPS51 subunit of the GARP and EARP complexesDavid C Gershlick, Morié Ishida, Julie R Jones, et al.Human Molecular Genetics|August 24, 2012
Functional characterization of tissue-specific enhancers in the DLX5/6 locusRamon Y Birnbaum, David B Everman, Karl K Murphy, et al.BMC Medical Genetics|July 28, 2007
Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypesRavinesh A Kumar, David B Everman, Chad T Morgan, et al.Journal of Child Neurology|July 29, 2008
Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic familyClaudia Amador, Anne M Mathews, Maria Del Carmen Montoya, et al.BMC Genomics|July 23, 2004
The FU gene and its possible protein isoformsTorben Østerlund, David B Everman, Regina C Betz, et al.Journal of Cell Science|November 24, 2021
Structural model of human PORCN illuminates disease-associated variants and drug-binding sitesJia Yu, Pei-Ju Liao, Weijun Xu, et al.Human Genetics|June 15, 2007
A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocationChristian Babbs, Raoul Heller, David B Everman, et al.Pageof 5