(Q28118961)
Statements
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Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism (English)
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Uma Mallya
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Mireille Castanet
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Maura Agostini
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Erik Schoenmakers
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Catherine Mitchell
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Stephanie Demuth
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F. Lucy Raymond
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John Schwabe
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Mark Gurnell
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V. Krishna Chatterjee
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