Thyroid dysgenesis (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Thyroid dysgenesis" in English language version.

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doi.org

  • Castanet M, Park SM, Smith A, et al. (August 2002). "A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate". Hum. Mol. Genet. 11 (17): 2051–9. doi:10.1093/hmg/11.17.2051. PMID 12165566.
  • Macchia PE, Lapi P, Krude H, et al. (May 1998). "PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis". Nat. Genet. 19 (1): 83–6. doi:10.1038/ng0598-83. PMID 9590296. S2CID 33957230.

medscape.com

emedicine.medscape.com

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Castanet M, Park SM, Smith A, et al. (August 2002). "A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate". Hum. Mol. Genet. 11 (17): 2051–9. doi:10.1093/hmg/11.17.2051. PMID 12165566.
  • Macchia PE, Lapi P, Krude H, et al. (May 1998). "PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis". Nat. Genet. 19 (1): 83–6. doi:10.1038/ng0598-83. PMID 9590296. S2CID 33957230.

oxfordjournals.org

hmg.oxfordjournals.org

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

semanticscholar.org

api.semanticscholar.org

  • Macchia PE, Lapi P, Krude H, et al. (May 1998). "PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis". Nat. Genet. 19 (1): 83–6. doi:10.1038/ng0598-83. PMID 9590296. S2CID 33957230.