Characterization of a novel loss of function mutation of PAX8 in a familial case of congenital hypothyroidism with in-place, normal-sized thyroid (Q24303392)

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Characterization of a novel loss of function mutation of PAX8 in a familial case of congenital hypothyroidism with in-place, normal-sized thyroid
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    Characterization of a novel loss of function mutation of PAX8 in a familial case of congenital hypothyroidism with in-place, normal-sized thyroid (English)
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    Laurent Meeus
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    Brigitte Gilbert
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    Catherine Rydlewski
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    Jasmine Parma
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    Anne Lienhardt Roussie
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    Marc Abramowicz
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    Catheline Vilain
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    Daniel Christophe
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    September 2004
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    89
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    9
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    4285-91
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