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5. Novel NKX2.1 mutation associated with hypothyroidism and lethal respiratory failure in a full-term neonate. Gillett ES; Deutsch GH; Bamshad MJ; McAdams RM; Mann PC J Perinatol; 2013 Feb; 33(2):157-60. PubMed ID: 23361500 [TBL] [Abstract][Full Text] [Related]
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