Síndrome CHARGE (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Síndrome CHARGE" in Spanish language version.

refsWebsite

Global rank Spanish rank

4^th place

2^nd place

6^th place

5^th place

low place

5,815^th place

491^st place

archive.org

Hall BD (1979). «Choanal atresia and associated multiple anomalies». J. Pediatr. 95 (3): 395-8. PMID 469662. doi:10.1016/S0022-3476(79)80513-2.
Pagon RA, Graham JM, Zonana J, Yong SL (1981). «Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association». J. Pediatr. 99 (2): 223-7. PMID 6166737. doi:10.1016/S0022-3476(81)80454-4.
Vissers, L. E., van Ravenswaaij, C. M., Admiraal, R., Hurst, J. A., de Vries, B. B., Janssen, I. M., et al. (2004). «Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.». Nature Genetics 36 (9): 955-957. PMID 15300250. doi:10.1038/ng1407.
Lalani SR, Safiullah AM, Fernbach SD, et al. (2006). «Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation». Am. J. Hum. Genet. 78 (2): 303-14. PMC 1380237. PMID 16400610. doi:10.1086/500273.

Usman, Norina; Sur, Moushumi (2022). CHARGE Syndrome. StatPearls Publishing. Consultado el 5 de marzo de 2022.
Hall BD (1979). «Choanal atresia and associated multiple anomalies». J. Pediatr. 95 (3): 395-8. PMID 469662. doi:10.1016/S0022-3476(79)80513-2.
Hittner HM, Hirsch NJ, Kreh GM, Rudolph AJ (1979). «Colobomatous microphthalmia, heart disease, hearing loss, and mental retardation--a syndrome». Journal of pediatric ophthalmology and strabismus 16 (2): 122-8. PMID 458518.
Pagon RA, Graham JM, Zonana J, Yong SL (1981). «Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association». J. Pediatr. 99 (2): 223-7. PMID 6166737. doi:10.1016/S0022-3476(81)80454-4.
Vissers, L. E., van Ravenswaaij, C. M., Admiraal, R., Hurst, J. A., de Vries, B. B., Janssen, I. M., et al. (2004). «Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.». Nature Genetics 36 (9): 955-957. PMID 15300250. doi:10.1038/ng1407.
Lalani SR, Safiullah AM, Fernbach SD, et al. (2006). «Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation». Am. J. Hum. Genet. 78 (2): 303-14. PMC 1380237. PMID 16400610. doi:10.1086/500273.