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

• Egile Nagusiak: Haque Sayedul (Egilea), Phadke Shubha R (Egilea), Roy Akhilesh K (Egilea), Wajid Muhammad (Egilea), Girisha KM (Egilea), Malik Sajid (Egilea), Ahmad Wasim (Egilea), Koch Manuela C (Egilea), Grzeschik Karl-Heinz (Egilea)
• Formatua: Liburua
• Argitaratua: BMC, 2007-12-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: 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...