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Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region

✍ Scribed by Robert Lyle; Uppala Radhakrishna; Jean-Louis Blouin; Sarantis Gagos; David B. Everman; Corinne Gehrig; Celia Delozier-Blanchet; Jitendra V. Solanki; Uday C. Patel; Swapan K. Nath; Fiorella Gurrieri; Giovanni Neri; Charles E. Schwartz; Stylianos E. Antonarakis

Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 449 KB
Volume: 140A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.31247

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## Abstract Split‐hand/foot malformation (SHFM), or ectrodactyly, is characterized by underdeveloped or absent central digital rays, clefts of the hands and feet, and variable syndactyly of the remaining digits. SHFM occurs as both an isolated finding and a component of many syndromes. SHFM is a he