Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

✍ Scribed by Lam, Wayne W K (author);Hatada, Izuho (author);Ohishi, Sachiko (author);Mukai, Tsunehiro (author);Joyce, Johanna A (author);Cole, Trevor R P (author);Donnai, Dian (author);Reik, Wolf (author);Schofield, Paul N (author);Maher, Eamonn R (author)

• Book ID: 121796580
• Publisher: BMJ
• Year: 1999
• Tongue: English
• Weight: 161 KB
• Volume: 36
• Category: Article
• ISSN: 0022-2593
• DOI: 10.1136/jmg.36.7.518