Associated Papers
Unraveling the Genetic Architecture of Hepatoblastoma Risk: Birth Defects and Increased Burden of Germline Damaging Variants in Gastrointestinal/Renal Cancer Predisposition and DNA Repair Genes.
Aguiar T et al.
Frontiers in Genetics, 2022
35495172 (PubMed )
Supplement: DataSheet1.xlsx › Supp_table_3
Plating human iPSC lines on micropatterned substrates reveals role for ITGB1 nsSNV in endoderm formation.
Vickers A et al.
Stem Cell Reports, 2021
34678211 (PubMed )
Supplement: mmc3.xlsx › Sheet1
Molecular analysis of the Noggin (NOG) gene in holoprosencephaly patients.
Srivastava K et al.
Molecular Genetics and Metabolism, 2012
A novel mutation in the gene encoding noggin is not causative in human neural tube defects.
Bauer KA et al.
Journal of Neurogenetics, 0
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