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Maternal isodisomy for a novel human FOXE1 gene mutation in syndromic congenital hypothyroidsim
Maternal isodisomy for a novel human FOXE1 gene mutation in syndromic congenital hypothyroidsim
2008
Mireille Castanet
Uma Mallya
Maura Agostini
Catherine Mitchell
Michel Polak
Stephanie Demuth
Lucy Raymond
Mark Gurnell
Krishna Chatterjee
Keywords:
Genetics
FOXE1 gene
Isodisomy
Mutation
Biology
Correction
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