Associated Papers
Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?
Ferrari L et al.
European Journal of Human Genetics : Ejhg, 2020
Whole exome sequencing in thrombophilic pedigrees to identify genetic risk factors for venous thromboembolism.
Cunha MLR et al.
Plos One, 2017
29117201 (PubMed )
Supplement: pone.0187699.s002.xlsx › SNPs_result_filter_strategies
Somatic signature of brain-specific single nucleotide variations in sporadic Alzheimer's disease.
Parcerisas A et al.
Journal of Alzheimer's Disease : Jad, 2014
25024348 (PubMed )
Supplement: sj-xls-6-alz-10.3233_jad-140891.xls › P3H
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