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S11011-016-9827-9
S11011-016-9827-9
http://dx.doi.org/10.1007/S11011-016-9827-9
Novel mutations in WWOX, RARS2, and C10orf2 genes in consanguineous Arab families with intellectual disability.
P356
Q48788494-E7B1F82E-9BD6-49C1-A098-08C18C742A26
P356
S11011-016-9827-9
http://dx.doi.org/10.1007/S11011-016-9827-9