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<p>disorders occur in individuals who are <a href="page.php?w=homozygous">homozygous</a> for a particular recessive gene <a href="page.php?w=mutation">mutation</a>. This means that they carry two copies (<a href="page.php?w=allele">allele</a>s) of the same gene. Except in certain rare circumstances (new mutations or <a href="page.php?w=uniparental_disomy">uniparental disomy</a>) both parents of an individual with such a disorder will be carriers of the gene. Such carriers are not affected and will not display any signs that they are carriers, and</p><p>
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