Preliminary candidate variants genotyping and distribution through the members of the reported family.</p
<p>The representative results of the genotypes provided by PCR-RFLP and sequencing.</p
Distribution of mutations according to their functional category among the validation cohort.</p
<p>Nucleotide variant information for re-sequencing projects conducted in current study.</p
Genotype distribution of the genetic variants investigated, expressed in percentages.</p
Variants found in the present study and clinical characteristics of the families.</p
<p>Variant Genotypes Created, Binary Codes, Substitutions and (Names of Genotypes Identified in Clin...
<p>The distribution of minor allele frequency of valid variants calls by genotyping by sequencing.</...
Primer sequences, fragment size, and genotyping method for the genotyped mutations.</p
<p>Distribution of the identified genotypes by family and frequency among the drug-susceptible pheno...
<p>Summary of five candidate variants with a consistent inheritance pattern detected by whole exome ...
<p>The distribution of heterozygosity of valid variants after genotyping by sequencing pipeline.</p
Percent distribution of monogenic variants identified in genes according to the CH phenotype.</p
Summary of the 26 variants remaining after filtering analysis of family CRC1.</p
<p>Total variants detected and number of variants per allele number at that locus.</p
Number of variants and genotyping rates for SNP datasets generated in this study.</p
<p>The representative results of the genotypes provided by PCR-RFLP and sequencing.</p
Distribution of mutations according to their functional category among the validation cohort.</p
<p>Nucleotide variant information for re-sequencing projects conducted in current study.</p
Genotype distribution of the genetic variants investigated, expressed in percentages.</p
Variants found in the present study and clinical characteristics of the families.</p
<p>Variant Genotypes Created, Binary Codes, Substitutions and (Names of Genotypes Identified in Clin...
<p>The distribution of minor allele frequency of valid variants calls by genotyping by sequencing.</...
Primer sequences, fragment size, and genotyping method for the genotyped mutations.</p
<p>Distribution of the identified genotypes by family and frequency among the drug-susceptible pheno...
<p>Summary of five candidate variants with a consistent inheritance pattern detected by whole exome ...
<p>The distribution of heterozygosity of valid variants after genotyping by sequencing pipeline.</p
Percent distribution of monogenic variants identified in genes according to the CH phenotype.</p
Summary of the 26 variants remaining after filtering analysis of family CRC1.</p
<p>Total variants detected and number of variants per allele number at that locus.</p
Number of variants and genotyping rates for SNP datasets generated in this study.</p
<p>The representative results of the genotypes provided by PCR-RFLP and sequencing.</p
Distribution of mutations according to their functional category among the validation cohort.</p
<p>Nucleotide variant information for re-sequencing projects conducted in current study.</p