Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily
Elena G. Bochukova, Tony Roscioli, Dale J. Hedges, Indira B. Taylor, David Johnson, David J. David, Prescott L. Deininger, Andrew O.M. WilkieVolume:
30
Year:
2009
Language:
english
Pages:
8
DOI:
10.1002/humu.20825
File:
PDF, 351 KB
english, 2009