Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences

• Main Authors: Haque Sayedul (Author), Phadke Shubha R (Author), Roy Akhilesh K (Author), Wajid Muhammad (Author), Girisha KM (Author), Malik Sajid (Author), Ahmad Wasim (Author), Koch Manuela C (Author), Grzeschik Karl-Heinz (Author)
• Format: Book
• Published: BMC, 2007-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Type II syndactyly or synpolydactyly (SPD) is clinically very heterogeneous, and genetically three distinct SPD conditions are known and have been designated as SPD1, SPD2 and SPD3, respectively. SPD1 type is associated with expansio...