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Hennie Bikker

7

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Clinical Reasoning: Heart to swallow

2016 Neurology
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NKX2-1 mutations in brain-lung-thyroid syndrome: a case series of four patients

2014 Journal of Pediatric Endocrinology and Metabolism
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A new PAX8 mutation causing congenital hypothyroidism in three generations of a family is associated with abnormalities in the urogenital tract.

2013 Thyroid
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