Deletions of exons with regulatory activity at theDYNC1I1locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families
Naeimeh Tayebi,Aleksander Jamsheer,Ricarda Flöttmann…Volume:
9
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-014-0108-6
Date:
December, 2014
File:
PDF, 1.11 MB
english, 2014