Norman–Roberts syndrome (English Wikipedia)

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

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Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA (2000). "Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations". Nature Genetics. 26 (1): 93–96. doi:10.1038/79246. PMID 10973257. S2CID 67748801.
Norman MG, Roberts M, Sirois J, Tremblay LJ (1976). "Lissencephaly". Canadian Journal of Neurological Sciences. 3 (1): 39–46. doi:10.1017/S0317167100025981. PMID 175907.

Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA (2000). "Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations". Nature Genetics. 26 (1): 93–96. doi:10.1038/79246. PMID 10973257. S2CID 67748801.
Norman MG, Roberts M, Sirois J, Tremblay LJ (1976). "Lissencephaly". Canadian Journal of Neurological Sciences. 3 (1): 39–46. doi:10.1017/S0317167100025981. PMID 175907.

Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA (2000). "Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations". Nature Genetics. 26 (1): 93–96. doi:10.1038/79246. PMID 10973257. S2CID 67748801.