Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 gene.
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J. Parma | S. Costagliola | A. Payot | C. Christophe-Hobertus | G. Vassart | Y. Robitaille | J. Fournet | L. Oligny | Emilie Maquet | S. Laberge | J. Deladoëy | G. Van Vliet | J. Vuissoz