Nature, Volume 456Sir Norman Lockyer Macmillan Journals Limited, 2008 |
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Página 62
... alleles differ from the reference and also differ from one another ) . The number of GA sequencing sites that are consistent with genotyping at both alleles , at one allele , or that are inconsistent at both alleles were categorized as ...
... alleles differ from the reference and also differ from one another ) . The number of GA sequencing sites that are consistent with genotyping at both alleles , at one allele , or that are inconsistent at both alleles were categorized as ...
Página 64
... alleles of 116 genes in the YH genome in the Online Mendelian Inheritance in Man ( OMIM ) 18 database and found one mutation in the GJB2 gene , which is associated with a recessive deafness disorder . This allele was het- erozygous ...
... alleles of 116 genes in the YH genome in the Online Mendelian Inheritance in Man ( OMIM ) 18 database and found one mutation in the GJB2 gene , which is associated with a recessive deafness disorder . This allele was het- erozygous ...
Página 722
... alleles of the causal gene ( multiple colours ) makes naive GWA scans ( such as in a ) ineffective . c , GWA scans miss rarely occurring alleles that have a large effect ( the top locus ) but locate common alleles with smaller effects ...
... alleles of the causal gene ( multiple colours ) makes naive GWA scans ( such as in a ) ineffective . c , GWA scans miss rarely occurring alleles that have a large effect ( the top locus ) but locate common alleles with smaller effects ...
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