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Author Details

Edward J Lose
The University of Alabama at Birmingham School of Medicine
1991
21
14
PMIDPaper TitleJournal TitlePublished Year
33843487The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child's Best Possible Life.AJOB Empir Bioeth2021
31250568Menkes disease complicated by concurrent Koolen-de Vries syndrome (17q21.31 deletion).Mol Genet Genomic Med2019
29652076Systematic reanalysis of genomic data improves quality of variant interpretation.Clin Genet2018
30302899Schaaf-Yang syndrome overview: Report of 78 individuals.Am J Med Genet A2018
29636925A case report of chromosome 17q22-qter trisomy with distinct clinical presentation and review of the literature.Clin Case Rep2018
29790872Genomic sequencing identifies secondary findings in a cohort of parent study participants.Genet Med2018
27561086Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results.Genet Med2017
28554332Genomic diagnosis for children with intellectual disability and/or developmental delay.Genome Med2017
28017373Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism.Am J Hum Genet2017
27841880The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.Nat Genet2017
27632688Clinical relevance of small copy-number variants in chromosomal microarray clinical testing.Genet Med2017
26385305Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States.Mol Genet Metab2015
21340693BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome.Hum Genet2011
22031302Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders.Am J Med Genet A2011
19282773AsktheGeneticist: five years of online experience.Genet Med2009
19533774Molecular cytogenetic characterization of two cases with constitutional distal 11q duplication/triplication.Am J Med Genet A2009
18203192The use by Alabama pediatricians of genetics consultation in the evaluation of developmental delay.Am J Med Genet A2008
19005331The emerging role of primary care in genetics.Curr Opin Pediatr2008
18025925Caring for adults with pediatric genetic diseases: a growing need.Curr Opin Pediatr2007
1335744Biology of the syndecans: a family of transmembrane heparan sulfate proteoglycans.Annu Rev Cell Biol1992
1769649Chromosome mapping of the murine syndecan gene.Genomics1991
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Collaborators

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Maastricht University Medical Centre
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University of Michigan ann arbor
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Baylor College of Medicine
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