Walker–Warburg syndrome (English Wikipedia)

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

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disabled-world.com

Weiss TC (1 February 2023) [6 March 2010]. "Walker-Warburg Syndrome - Facts and Information". Disabled World.

Vajsar J, Schachter H (August 2006). "Walker-Warburg syndrome". Orphanet Journal of Rare Diseases. 1: 29. doi:10.1186/1750-1172-1-29. PMC 1553431. PMID 16887026.
Beltrán-Valero de Bernabé D, Currier S, Steinbrecher A, Celli J, van Beusekom E, van der Zwaag B, et al. (November 2002). "Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome". American Journal of Human Genetics. 71 (5): 1033–1043. doi:10.1086/342975. PMC 419999. PMID 12369018.
Maroofian R, Riemersma M, Jae LT, Zhianabed N, Willemsen MH, Wissink-Lindhout WM, et al. (December 2017). "B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies". Genome Medicine. 9 (1): 118. doi:10.1186/s13073-017-0505-2. PMC 5740572. PMID 29273094.
Vajsar J, Schachter H (August 2006). "Walker-Warburg syndrome". Orphanet Journal of Rare Diseases. 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.

"Walker-Warburg syndrome". MedlinePlus Genetics. U.S. National Library of Medicine. Retrieved 2023-03-14.

Vajsar J, Schachter H (August 2006). "Walker-Warburg syndrome". Orphanet Journal of Rare Diseases. 1: 29. doi:10.1186/1750-1172-1-29. PMC 1553431. PMID 16887026.
Beltrán-Valero de Bernabé D, Currier S, Steinbrecher A, Celli J, van Beusekom E, van der Zwaag B, et al. (November 2002). "Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome". American Journal of Human Genetics. 71 (5): 1033–1043. doi:10.1086/342975. PMC 419999. PMID 12369018.
Maroofian R, Riemersma M, Jae LT, Zhianabed N, Willemsen MH, Wissink-Lindhout WM, et al. (December 2017). "B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies". Genome Medicine. 9 (1): 118. doi:10.1186/s13073-017-0505-2. PMC 5740572. PMID 29273094.
Vajsar J, Schachter H (August 2006). "Walker-Warburg syndrome". Orphanet Journal of Rare Diseases. 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 Original Article Series. 7 (3): 136–154. PMID 4950916.

"Walker-Warburg syndrome". Genetic and Rare Diseases Information Center (GARD) – an NCATS Program. U.S. National Institutes of Health. Retrieved 2018-04-09.

"Walker-Warburg syndrome". Genetics Home Reference. U.S. National Library of Medicine. Retrieved 2018-04-17.