Associated Papers
Rare Tumor-Normal Matched Whole Exome Sequencing Identifies Novel Genomic Pathogenic Germline and Somatic Aberrations.
Sprissler R et al.
Cancers, 2020
32570879 (PubMed )
Supplement: cancers-12-01618-s001.zip › cancers-817200-Supplementary_Materials3 › Supplementary_table_S1.xlsx › TSG
Application of next-generation sequencing for the diagnosis of fetuses with congenital heart defects.
Qiao F et al.
Current Opinion in Obstetrics & Gynecology, 2019
Bond swapping from a charge cloud allows flexible coordination of upstream signals through WASP: Multiple regulatory roles for the WASP basic region.
Tetley GJN et al.
The Journal of Biological Chemistry, 2018
Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound.
Carss KJ et al.
Human Molecular Genetics, 2014
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