4 results on '"Serra, Eva G."'
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2. Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
3. Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ
4. Frequent occurrence of DUOX2 and DUOXA2 mutations in cases with borderline bloodspot screening TSH who develop 'True' congenital hypothyroidism
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