Thyroid dyshormonogenesis (English Wikipedia)

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

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Avbelj M, Tahirovic H, Debeljak M, et al. (May 2007). "High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis". Eur. J. Endocrinol. 156 (5): 511–9. doi:10.1530/EJE-07-0037. PMID 17468186.
Grasberger, Helmut; Refetoff, Samuel (August 2011). "Genetic causes of congenital hypothyroidism due to dyshormonogenesis". Current Opinion in Pediatrics. 23 (4): 421. doi:10.1097/MOP.0b013e32834726a4. ISSN 1040-8703. PMC 3263319.
Sheffield, Val C.; Kraiem, Zaki; Beck, John C.; Nishimura, Darryl; Stone, Edwin M.; Salameh, Muhamad; Sadeh, Orit; Glaser, Benjamin (April 1996). "Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification". Nature Genetics. 12 (4): 424–426. doi:10.1038/ng0496-424. ISSN 1546-1718.

Kumar PG, Anand SS, Sood V, Kotwal N (December 2005). "Thyroid dyshormonogenesis" (PDF). Indian Pediatr. 42 (12): 1233–5. PMID 16424561.

Sheffield, Val C.; Kraiem, Zaki; Beck, John C.; Nishimura, Darryl; Stone, Edwin M.; Salameh, Muhamad; Sadeh, Orit; Glaser, Benjamin (April 1996). "Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification". Nature Genetics. 12 (4): 424–426. doi:10.1038/ng0496-424. ISSN 1546-1718.

Avbelj M, Tahirovic H, Debeljak M, et al. (May 2007). "High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis". Eur. J. Endocrinol. 156 (5): 511–9. doi:10.1530/EJE-07-0037. PMID 17468186.
Kumar PG, Anand SS, Sood V, Kotwal N (December 2005). "Thyroid dyshormonogenesis" (PDF). Indian Pediatr. 42 (12): 1233–5. PMID 16424561.

Grasberger, Helmut; Refetoff, Samuel (August 2011). "Genetic causes of congenital hypothyroidism due to dyshormonogenesis". Current Opinion in Pediatrics. 23 (4): 421. doi:10.1097/MOP.0b013e32834726a4. ISSN 1040-8703. PMC 3263319.
Sheffield, Val C.; Kraiem, Zaki; Beck, John C.; Nishimura, Darryl; Stone, Edwin M.; Salameh, Muhamad; Sadeh, Orit; Glaser, Benjamin (April 1996). "Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification". Nature Genetics. 12 (4): 424–426. doi:10.1038/ng0496-424. ISSN 1546-1718.