Associated Papers
Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology.
Moresco G et al.
Genes & Genomics, 2023
Family studies to find rare high risk variants in migraine.
Hansen RD et al.
The Journal of Headache and Pain, 2017
A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment.
Nyegaard M et al.
Plos Genetics, 2015
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