Results of complex segregation analysis using regressive logistic models for LS in the Lundehund. (DOCX 12 kb
Additional variants in the couples. Additional file describing additional possibly pathogenic varian...
A scatter plot showing correlation of percent of homozygosity with the number of homozygous likely g...
Non-syndromic hearing loss phenotype - linkage plot showing logarithm of odds (LOD) scores across th...
Private runs of homozygosity for LS-unaffected Lundehund in 500-SNP windows. The chromosomal positio...
Runs of homozygosity for Lundehund specific regions in 500-SNP windows. The chromosomal position of ...
Primer sequences used for genotyping of candidate SNPs. The two variants located in KRT3 and LEPREL1...
Table S4. Primers for sequencing the regions, containing DArTseq-derived SNPs. (XLSX 343 kb
A screen-shot of VIKING showing variants identified by DRAGEN in WGS26 of sample UDT_103, a patient ...
WES statistics. Number of genetic variants called after the WES analysis. (DOCX 15 kb
Distribution of all variants (a) and variants with likely pathogenic effect (b) by gene. Frequency o...
Output data from the linkage analysis in the L084 family with X-linked intellectual disability. (LOG...
Output data from the linkage analysis in the L061 family with X-linked intellectual disability. (LOG...
Pairwise linkage disequilibrium (LD) of associated variants. A list of detected genetic variants fou...
Output data from the linkage analysis in the L020 family with X-linked intellectual disability. (LOG...
Supplementary Methods: Description of methods for pooled variant calling, gene-level tests for rare ...
Additional variants in the couples. Additional file describing additional possibly pathogenic varian...
A scatter plot showing correlation of percent of homozygosity with the number of homozygous likely g...
Non-syndromic hearing loss phenotype - linkage plot showing logarithm of odds (LOD) scores across th...
Private runs of homozygosity for LS-unaffected Lundehund in 500-SNP windows. The chromosomal positio...
Runs of homozygosity for Lundehund specific regions in 500-SNP windows. The chromosomal position of ...
Primer sequences used for genotyping of candidate SNPs. The two variants located in KRT3 and LEPREL1...
Table S4. Primers for sequencing the regions, containing DArTseq-derived SNPs. (XLSX 343 kb
A screen-shot of VIKING showing variants identified by DRAGEN in WGS26 of sample UDT_103, a patient ...
WES statistics. Number of genetic variants called after the WES analysis. (DOCX 15 kb
Distribution of all variants (a) and variants with likely pathogenic effect (b) by gene. Frequency o...
Output data from the linkage analysis in the L084 family with X-linked intellectual disability. (LOG...
Output data from the linkage analysis in the L061 family with X-linked intellectual disability. (LOG...
Pairwise linkage disequilibrium (LD) of associated variants. A list of detected genetic variants fou...
Output data from the linkage analysis in the L020 family with X-linked intellectual disability. (LOG...
Supplementary Methods: Description of methods for pooled variant calling, gene-level tests for rare ...
Additional variants in the couples. Additional file describing additional possibly pathogenic varian...
A scatter plot showing correlation of percent of homozygosity with the number of homozygous likely g...
Non-syndromic hearing loss phenotype - linkage plot showing logarithm of odds (LOD) scores across th...
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