bibliographic entry 12697173 [be/12697173]
https://w3id.org/oc/corpus/be/12697173
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Stasia, M.J, Mollin, M, Martel, C. Functional and genetic characterization of two extremely rare cases of WilliamsâBeuren syndrome associated with chronic granulomatous disease, Eur. J. Hum. Genet, 21, 2013, 1079, 1084, PMID: 23340515
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