Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention
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Z. Kibar | F. Magne | A. Petryk | J. Deladoëy | G. Van Vliet | S. Larrivée-Vanier | Elwaseila Hamdoun
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Z. Kibar | F. Magne | A. Petryk | J. Deladoëy | G. Van Vliet | S. Larrivée-Vanier | Elwaseila Hamdoun