Sindrom Coffin-Lowry (Malay Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sindrom Coffin-Lowry" in Malay language version.

refsWebsite

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low place

1whonamedit.com

2,888^th place

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262^nd place

2^nd place

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doi.org

Delaunoy JP, Dubos A, Marques Pereira P, Hanauer A (2006). "Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome". Clin. Genet. 70 (2): 161–6. doi:10.1111/j.1399-0004.2006.00660.x. PMID 16879200. Unknown parameter |month= ignored (bantuan)CS1 maint: multiple names: authors list (link)

nih.gov

pubmed.ncbi.nlm.nih.gov

Lowry B, Miller JR, Fraser FC (1971). "A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus". Am. J. Dis. Child. 121 (6): 496–500. PMID 5581017. Unknown parameter |month= ignored (bantuan)CS1 maint: multiple names: authors list (link)
Delaunoy JP, Dubos A, Marques Pereira P, Hanauer A (2006). "Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome". Clin. Genet. 70 (2): 161–6. doi:10.1111/j.1399-0004.2006.00660.x. PMID 16879200. Unknown parameter |month= ignored (bantuan)CS1 maint: multiple names: authors list (link)

whonamedit.com

synd/3425 di Who Named It?

wikipedia.org

en.wikipedia.org

Lowry B, Miller JR, Fraser FC (1971). "A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus". Am. J. Dis. Child. 121 (6): 496–500. PMID 5581017. Unknown parameter |month= ignored (bantuan)CS1 maint: multiple names: authors list (link)
Delaunoy JP, Dubos A, Marques Pereira P, Hanauer A (2006). "Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome". Clin. Genet. 70 (2): 161–6. doi:10.1111/j.1399-0004.2006.00660.x. PMID 16879200. Unknown parameter |month= ignored (bantuan)CS1 maint: multiple names: authors list (link)

wiley.com

onlinelibrary.wiley.com

Delaunoy JP, Dubos A, Marques Pereira P, Hanauer A (2006). "Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome". Clin. Genet. 70 (2): 161–6. doi:10.1111/j.1399-0004.2006.00660.x. PMID 16879200. Unknown parameter |month= ignored (bantuan)CS1 maint: multiple names: authors list (link)