Last Name


Search Results to Neil Miller

This is a "connection" page, showing the details of why an item matched the keywords from your search.


One or more keywords matched the following items that are connected to Miller, Neil

Item TypeName
Concept DNA Mutational Analysis
Concept Sequence Analysis, DNA
Concept Sequence Analysis, RNA
Concept Oligonucleotide Array Sequence Analysis
Concept Microarray Analysis
Academic Article Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
Academic Article Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.
Academic Article A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases.
Academic Article The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP) Allele Nomenclature Database.
Academic Article Clinical genome sequencing in an unbiased pediatric cohort.
Academic Article Adopting orphans: comprehensive genetic testing of Mendelian diseases of childhood by next-generation sequencing.
Academic Article Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome.
Academic Article Molecular diagnosis of infantile onset inflammatory bowel disease by exome sequencing.
Academic Article Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.
Academic Article PCDH19-related epileptic encephalopathy in a male mosaic for a truncating variant.
Academic Article Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease.
Academic Article CLPB variants associated with autosomal-recessive mitochondrial disorder with cataract, neutropenia, epilepsy, and methylglutaconic aciduria.
Academic Article Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report.
Academic Article MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates.
Academic Article Using dried blood spots for variant analysis for patients with haemophilia.
Academic Article C6/36 Aedes albopictus cells have a dysfunctional antiviral RNA interference response.
Academic Article Carrier testing for severe childhood recessive diseases by next-generation sequencing.
Academic Article Exome sequencing reveals a pallidin mutation in a Hermansky-Pudlak-like primary immunodeficiency syndrome.
Academic Article An integrated transcriptome and expressed variant analysis of sepsis survival and death.
Academic Article Genomic convergence analysis of schizophrenia: mRNA sequencing reveals altered synaptic vesicular transport in post-mortem cerebellum.
Academic Article A highly annotated whole-genome sequence of a Korean individual.
Academic Article Design, implementation and maintenance of a model organism database for Arabidopsis thaliana.
Academic Article The Arabidopsis Information Resource (TAIR): a model organism database providing a centralized, curated gateway to Arabidopsis biology, research materials and community.
Academic Article Visual loss after corrective surgery for pediatric scoliosis: incidence and risk factors from a nationwide database.

Search Criteria
  • Database
  • Analysis