Correction: Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families

समान संसाधन

• Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families
  द्वारा: Dai, Limeng, और अन्य
  प्रकाशित: (2014)
• Mutations in HOXD13 Underlie Syndactyly Type V and a Novel Brachydactyly-Syndactyly Syndrome
  द्वारा: Zhao, Xiuli , और अन्य
  प्रकाशित: (2007)
• Missense Mutations in the Homeodomain of HOXD13 Are Associated with Brachydactyly Types D and E
  द्वारा: Johnson, David, और अन्य
  प्रकाशित: (2003)
• A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family
  द्वारा: Zaib, Tahir, और अन्य
  प्रकाशित: (2019)
• Correction: Two Novel Mutations in Myosin Binding Protein C Slow Causing Distal Arthrogryposis Type 2 in Two Large Han Chinese Families May Suggest Important Functional Role of Immunoglobulin Domain C2
  प्रकाशित: (2015)