RWDD2B (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "RWDD2B" in English language version.

refsWebsite

Global rank English rank

4^th place

4^th place

1,626^th place

1,007^th place

2^nd place

2^nd place

doi.org (Global: 2^nd place; English: 2^nd place)

Orti R, Rachidi M, Vialard F, Toyama K, Lopes C, Taudien S, Rosenthal A, Yaspo ML, Sinet PM, Delabar JM (May 2000). "Characterization of a novel gene, C21orf6, mapping to a critical region of chromosome 21q22.1 involved in the monosomy 21 phenotype and of its murine ortholog, orf5". Genomics. 64 (2): 203–10. doi:10.1006/geno.1999.6109. PMID 10729227.

ensembl.org (Global: 1,626^th place; English: 1,007^th place)

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000156253 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000041079 – Ensembl, May 2017

nih.gov (Global: 4^th place; English: 4^th place)

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: C21orf6 chromosome 21 open reading frame 6".

pubmed.ncbi.nlm.nih.gov

Orti R, Rachidi M, Vialard F, Toyama K, Lopes C, Taudien S, Rosenthal A, Yaspo ML, Sinet PM, Delabar JM (May 2000). "Characterization of a novel gene, C21orf6, mapping to a critical region of chromosome 21q22.1 involved in the monosomy 21 phenotype and of its murine ortholog, orf5". Genomics. 64 (2): 203–10. doi:10.1006/geno.1999.6109. PMID 10729227.