Wadey, R., Mckie, J., Papapetrou, C., Sutherland, H., Lohman, F., Osinga, J., et al. (1999). Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1]. AMERICAN JOURNAL OF HUMAN GENETICS, 65(1), 247-249 [10.1086/302468].
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1]
AMATI, FRANCESCA;NOVELLI, GIUSEPPE;
1999-01-01
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