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Software and database for the analysis of mutations in the human WT1 gene., , , and . Nucleic Acids Research, 26 (1): 271-274 (1998)Correction: Dispelling myths about rare disease registry system development., , , , , , , , and . Source Code for Biology and Medicine, (2014)VarioML framework for comprehensive variation data representation and exchange., , , , , , , , , and 7 other author(s). BMC Bioinformatics, (2012)Software and database for the analysis of mutations in the VHL gene., , , , , and . Nucleic Acids Research, 26 (1): 256-258 (1998)LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis., , , , , , , , , and 10 other author(s). Nucleic Acids Research, 26 (1): 248-252 (1998)APC gene: database of germline and somatic mutations in human tumors and cell lines., and . Nucleic Acids Research, 24 (1): 121-124 (1996)Software and database for the analysis of mutations in the human FBN1 gene., , , , and . Nucleic Acids Research, 24 (1): 137-140 (1996)Software and database for the analysis of mutations in the human LDL receptor gene., , , , , and . Nucleic Acids Research, 25 (1): 172-180 (1997)VarAFT: a variant annotation and filtration system for human next generation sequencing data., , , , , , and . Nucleic Acids Research, 46 (Webserver-Issue): W545-W553 (2018)p53 gene mutation: software and database., and . Nucleic Acids Research, 26 (1): 200-204 (1998)