Associated Papers
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Iscience, 2022
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Supplement: mmc5.xlsx › DBD_missense_mutations
A novel missense mutation in TFAP2B associated with Char syndrome and central diabetes insipidus.
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American Journal of Medical Genetics. Part A, 2019
A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data.
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Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
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Supplement: gkn1008_nar-01723-s-2008-File009.xls › TypeII-
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