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Walker–Warburg syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Walker–Warburg syndrome" in English language version.

refsWebsite
Global rank English rank
9nih.gov
4th place
4th place
4doi.org
2nd place
2nd place
2whonamedit.com
2,888th place
2,730th place
1omim.org
4,380th place
4,305th place
1medlineplus.gov
1,581st place
1,299th place
1disabled-world.com
low place
low place

disabled-world.com

doi.org

  • Vajsar J, Schachter H (2006). "Walker–Warburg syndrome". Orphanet J Rare Dis. 1: 29. doi:10.1186/1750-1172-1-29. PMC 1553431. PMID 16887026.
  • Beltrán-Valero de Bernabé D, Currier S, Steinbrecher A, et al. (November 2002). "Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker–Warburg syndrome". Am. J. Hum. Genet. 71 (5): 1033–43. doi:10.1086/342975. PMC 419999. PMID 12369018.
  • Vajsar J, Schachter H (2006). "Walker-Warburg syndrome". Orphanet J Rare Dis. 1: 29. doi:10.1186/1750-1172-1-29. PMC 1553431. PMID 16887026.
  • Walker AE (1942). "Lissencephaly". Archives of Neurology and Psychiatry. 48: 13–29. doi:10.1001/archneurpsyc.1942.02290070023002.

medlineplus.gov

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Vajsar J, Schachter H (2006). "Walker–Warburg syndrome". Orphanet J Rare Dis. 1: 29. doi:10.1186/1750-1172-1-29. PMC 1553431. PMID 16887026.
  • Beltrán-Valero de Bernabé D, Currier S, Steinbrecher A, et al. (November 2002). "Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker–Warburg syndrome". Am. J. Hum. Genet. 71 (5): 1033–43. doi:10.1086/342975. PMC 419999. PMID 12369018.
  • Vajsar J, Schachter H (2006). "Walker-Warburg syndrome". Orphanet J Rare Dis. 1: 29. doi:10.1186/1750-1172-1-29. PMC 1553431. PMID 16887026.
  • Warburg M (March 1971). "The heterogeneity of microphthalmia in the mentally retarded". Birth Defects Orig. Artic. Ser. 7 (3): 136–54. PMID 4950916.

ncbi.nlm.nih.gov

  • Vajsar J, Schachter H (2006). "Walker–Warburg syndrome". Orphanet J Rare Dis. 1: 29. doi:10.1186/1750-1172-1-29. PMC 1553431. PMID 16887026.
  • Beltrán-Valero de Bernabé D, Currier S, Steinbrecher A, et al. (November 2002). "Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker–Warburg syndrome". Am. J. Hum. Genet. 71 (5): 1033–43. doi:10.1086/342975. PMC 419999. PMID 12369018.
  • Vajsar J, Schachter H (2006). "Walker-Warburg syndrome". Orphanet J Rare Dis. 1: 29. doi:10.1186/1750-1172-1-29. PMC 1553431. PMID 16887026.

rarediseases.info.nih.gov

ghr.nlm.nih.gov

omim.org

whonamedit.com