Disgenesia tiroidea (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Disgenesia tiroidea" in Italian language version.

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archive.org

Brad W. Neville , Douglas D. Damm, Carl M. Allen, Jerry E. Bouquot, Oral & maxillofacial pathology, 2. ed., Philadelphia, W.B. Saunders, 2002, pp. 11-12, ISBN 0-7216-9003-3.

doi.org

dx.doi.org

Castanet M, Park SM, Smith A, et al, A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate, in Hum. Mol. Genet., vol. 11, n. 17, agosto 2002, pp. 2051–9, DOI:10.1093/hmg/11.17.2051, PMID 12165566.
Macchia PE, Lapi P, Krude H, et al, PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis, in Nat. Genet., vol. 19, n. 1, maggio 1998, pp. 83–6, DOI:10.1038/ng0598-83, PMID 9590296.

medscape.com

emedicine.medscape.com

emedicine > Embryology of the Thyroid and Parathyroids > Thyroid Embryology Clinical Correlations By David J Kay and Arlen D Meyers. Updated: Jan 14, 2010

nih.gov

ncbi.nlm.nih.gov

Castanet M, Park SM, Smith A, et al, A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate, in Hum. Mol. Genet., vol. 11, n. 17, agosto 2002, pp. 2051–9, DOI:10.1093/hmg/11.17.2051, PMID 12165566.
Macchia PE, Lapi P, Krude H, et al, PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis, in Nat. Genet., vol. 19, n. 1, maggio 1998, pp. 83–6, DOI:10.1038/ng0598-83, PMID 9590296.

oadoi.org

Macchia PE, Lapi P, Krude H, et al, PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis, in Nat. Genet., vol. 19, n. 1, maggio 1998, pp. 83–6, DOI:10.1038/ng0598-83, PMID 9590296.

oxfordjournals.org

hmg.oxfordjournals.org

Castanet M, Park SM, Smith A, et al, A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate, in Hum. Mol. Genet., vol. 11, n. 17, agosto 2002, pp. 2051–9, DOI:10.1093/hmg/11.17.2051, PMID 12165566.