about
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-BPrecocious sister chromatid separation (PSCS) in Cornelia de Lange syndromeCopy number variation at 1q21.1 associated with neuroblastomaCommon variations in BARD1 influence susceptibility to high-risk neuroblastomaIdentification of ALK as a major familial neuroblastoma predisposition geneChromosome 6p22 locus associated with clinically aggressive neuroblastomaIRAK-M is involved in the pathogenesis of early-onset persistent asthmaAssociation of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's diseaseAssociation of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended FamilyAssociation of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's diseaseGenome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
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հետազոտող
@hy
name
Marcella Devoto
@ast
Marcella Devoto
@en
Marcella Devoto
@es
Marcella Devoto
@nl
Marcella Devoto
@sl
type
label
Marcella Devoto
@ast
Marcella Devoto
@en
Marcella Devoto
@es
Marcella Devoto
@nl
Marcella Devoto
@sl
prefLabel
Marcella Devoto
@ast
Marcella Devoto
@en
Marcella Devoto
@es
Marcella Devoto
@nl
Marcella Devoto
@sl