<style face="normal" font="default" size="100%">Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss.</style>

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<style face="normal" font="default" size="100%">Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss.</style>

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<style face="normal" font="default" size="100%">Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.</style>

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<style face="normal" font="default" size="100%">Phenotypic expression of 19q13.32 microdeletions: Report of a new patient and review of the literature.</style>

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<style face="normal" font="default" size="100%">Brain-derived neurotrophic factor serum levels in genetically isolated populations: gender-specific association with anxiety disorder subtypes but not with anxiety levels or Val66Met polymorphism.</style>

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<style face="normal" font="default" size="100%">Directional dominance on stature and cognition in diverse human populations.</style>

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<style face="normal" font="default" size="100%">Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss.</style>