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Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model
National licenceNature Publishing Group | 2008| -
Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons
National licenceNature Publishing Group | 2006| -
An integrative genomics approach to infer causal associations between gene expression and disease
National licenceNature Publishing Group | 2005| -
A high-resolution survey of deletion polymorphism in the human genome
National licenceNature Publishing Group | 2006| -
A wiki for the life sciences where authorship matters
National licenceNature Publishing Group | 2008| -
Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
National licenceNature Publishing Group | 2003| -
Ancestral reconstruction of segmental duplications reveals punctuated cores of human genome evolution
National licenceNature Publishing Group | 2007| -
An oncogenic KRAS2 expression signature identified by cross-species gene-expression analysis
National licenceNature Publishing Group | 2005| -
Erasure of MLH1 methylation in spermatozoa—implications for epigenetic inheritance
National licenceNature Publishing Group | 2007| -
Automating resequencing-based detection of insertion-deletion polymorphisms
National licenceNature Publishing Group | 2006| -
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
National licenceNature Publishing Group | 2000| -
Allegro, a new computer program for multipoint linkage analysis
National licenceNature Publishing Group | 2000| -
Interaction of reelin signaling and Lis1 in brain development
National licenceNature Publishing Group | 2003| -
Ptprj is a candidate for the mouse colon-cancer susceptibility locus Scc1 and is frequently deleted in human cancers
National licenceNature Publishing Group | 2002|
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