Associated Papers
Exome sequencing of a family with lone, autosomal dominant atrial flutter identifies a rare variation in ABCB4 significantly enriched in cases.
Maciąg A et al.
Bmc Genetics, 2015
25888430 (PubMed )
Supplement: 12863_2015_177_MOESM1_ESM.xls › Sheet1
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1843.647
Comprehensive genomic analysis of a BRCA2 deficient human pancreatic cancer.
Barber LJ et al.
Plos One, 2011
21750719 (PubMed )
Supplement: pone.0021639.s006.xls › Sheet1
Select a paper to view details