DOI:
10.1055/s-00034612
Yearbook of Medical Informatics
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References
Bragin E, Chatzimichali EA, Wright CF, Hurles ME, Firth HV, Bevan AP. , et al.
DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation.
Nucleic Acids Res 2014;
42 (Database issue): D993-D1000
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