DECIPHER (Romanian Wikipedia)

Analysis of information sources in references of the Wikipedia article "DECIPHER" in Romanian language version.

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doi.org

Firth HV, Richards SM, Bevan AP; et al. (aprilie 2009). „DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources”. Am. J. Hum. Genet. 84 (4): 524–33. doi:10.1016/j.ajhg.2009.03.010. PMC 2667985 . PMID 19344873.
Swaminathan GJ, Bragin E, Chatzimichali EA"; et al. (2012). „DECIPHER: web-based community resource for clinical interpretation of rare variants in developmental disorders”. Hum. Mol. Genet. R1 (R1): R37–R44. doi:10.1093/hmg/dds362. PMID 22962312.
Bragin E, Chatzimichali EA"; et al. (2014). „DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation”. Nucleic Acids Res. D1 (Database issue): D993–D1000. doi:10.1093/nar/gkt937. PMC 3965078 . PMID 24150940.
Niemitz, E (2009). „DECIPHERing chromosomal imbalances”. Nature Genetics. 41 (5): 514. doi:10.1038/ng0509-514.

Firth HV, Richards SM, Bevan AP; et al. (aprilie 2009). „DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources”. Am. J. Hum. Genet. 84 (4): 524–33. doi:10.1016/j.ajhg.2009.03.010. PMC 2667985 . PMID 19344873.
Swaminathan GJ, Bragin E, Chatzimichali EA"; et al. (2012). „DECIPHER: web-based community resource for clinical interpretation of rare variants in developmental disorders”. Hum. Mol. Genet. R1 (R1): R37–R44. doi:10.1093/hmg/dds362. PMID 22962312.
Bragin E, Chatzimichali EA"; et al. (2014). „DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation”. Nucleic Acids Res. D1 (Database issue): D993–D1000. doi:10.1093/nar/gkt937. PMC 3965078 . PMID 24150940.

„About DECIPHER”. Wellcome Trust Sanger Institute. Arhivat din original la 13 iunie 2018. Accesat în 12 februarie 2014.

„About DECIPHER”. Wellcome Trust Sanger Institute. Arhivat din original la 13 iunie 2018. Accesat în 12 februarie 2014.