Novel TBX3 mutation data in families with Ulnar–Mammary syndrome indicate a genotype–phenotype relationship: mutations that do not disrupt the T-domain are associated with less severe limb defects

✍ Scribed by Vasco Meneghini; Sylvie Odent; Natalia Platonova; Aliana Egeo; Giorgio R. Merlo

• Book ID: 116432807
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 160 KB
• Volume: 49
• Category: Article
• ISSN: 1769-7212
• DOI: 10.1016/j.ejmg.2005.04.021