Associated Papers
Börjeson-Forssman-Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new families.
Jain V et al.
European Journal of Human Genetics : Ejhg, 2023
37704779 (PubMed )
Supplement: 41431_2023_1447_MOESM5_ESM.xlsx › Supplementary_Table_4
SmMIP-tools: a computational toolset for processing and analysis of single-molecule molecular inversion probes-derived data.
Medeiros JJF et al.
Bioinformatics (oxford, England), 2022
35150236 (PubMed )
Supplement: btac081_supplementary_data.zip › Table_S6.xlsx › High_Confidence_SNVs
Next-generation sequencing in X-linked intellectual disability.
Tzschach A et al.
European Journal of Human Genetics : Ejhg, 2015
Select a paper to view details