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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1989 1
1990 1
1991 2
1993 1
1995 2
2009 1
2010 1
2024 0

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PubMed for id: 1383394

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Page 1
Molecular analysis of congenital goitres with hypothyroidism caused by defective thyroglobulin synthesis. Identification of a novel c.7006C>T [p.R2317X] mutation and expression of minigenes containing nonsense mutations in exon 7.
Machiavelli GA, Caputo M, Rivolta CM, Olcese MC, Gruñeiro-Papendieck L, Chiesa A, González-Sarmiento R, Targovnik HM. Machiavelli GA, et al. Clin Endocrinol (Oxf). 2010 Jan;72(1):112-21. doi: 10.1111/j.1365-2265.2009.03621.x. Epub 2009 May 2. Clin Endocrinol (Oxf). 2010. PMID: 19438905