<style face="normal" font="default" size="100%">Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families.</style>

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<style face="normal" font="default" size="100%">Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families.</style>

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<style face="normal" font="default" size="100%">Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar.</style>

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<style face="normal" font="default" size="100%">The p.Cys169Tyr variant of connexin 26 is not a polymorphism.</style>

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<style face="normal" font="default" size="100%">Consanguinity and hereditary hearing loss in Qatar.</style>