论文信息 - Functional and genetic characterization of two extremely rare cases of Williams–Beuren Syndrome associated with chronic granulomatous disease - 字舞流文

Functional and genetic characterization of two extremely rare cases of Williams–Beuren Syndrome associated with chronic granulomatous disease

J. Brion | D. Roos | C. Coutton | C. Martel | V. Satre | M. Stasia | J. Boelens | G. Vieville | H. Veenstra-Knol | M. Boer | F. Amblard | Michéle Mollin | J. Montfrans | KarenM. van Leeuwen | K. V. Leeuwen