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500273
500273
http://dx.doi.org/10.1086/500273
Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.
P356
Q24540535-F955698D-BED0-4508-821B-AE95D8D4C686
P356
500273
http://dx.doi.org/10.1086/500273