Wikidata

(Q58666635)

English

Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted

article

In more languages

Statements

title
Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8518793
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8518793%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
author name string

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    Retrieved from "https://www.wikidata.org/w/index.php?title=Q58666635&oldid=2137091168"