Sign In

Login

Password

Forgot Password ? Sign Up

Lethal congenital contracture syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Lethal congenital contracture syndrome" in English language version.

refsWebsite
Global rank English rank
8nih.gov
4th place
4th place
6doi.org
2nd place
2nd place
2semanticscholar.org
11th place
8th place
1omim.org
4,380th place
4,305th place

doi.org

  • Norio R (2003). "The Finnish disease heritage III: the individual diseases". Hum. Genet. 112 (5–6): 486–487. doi:10.1007/s00439-002-0877-1. PMID 12627297. S2CID 26741302.
  • Herva R, Leisti J, Kirkinen P, Seppänen U (1985). "A lethal autosomal recessive syndrome of multiple congenital contractures". Am. J. Med. Genet. 20 (3): 431–439. doi:10.1002/ajmg.1320200303. PMID 3993672.
  • Herva R, Conradi N, Kalimo H, Leisti J, Sourander P (1988). "A lethal autosomal recessive syndrome of multiple congenital contractures. Neuropathological analysis of five fetal cases". Am. J. Med. Genet. 29 (1): 67–76. doi:10.1002/ajmg.1320290109. PMID 3344776.
  • Nousiainen HO, Kestilä M, Pakkasjärvi N, Honkala H, Kuure S, Tallila J, Vuopala K, Ignatius J, Herva R, Peltonen L (2008). "Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease". Nature Genetics. 40 (2): 155–157. doi:10.1038/ng.2007.65. PMC 2684619. PMID 18204449.
  • Nousiainen HO, Kestilä M, Pakkasjärvi N, Honkala H, Kuure S, Tallila J, Vuopala K, Ignatius J, Herva R, Peltonen L (February 2008). "Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease". Nature Genetics. 40 (2): 155–157. doi:10.1038/ng.2007.65. PMC 2684619. PMID 18204449.
  • Pakkasjärvi N, Ritvanen A, Herva R, Peltonen L, Kestilä M, Ignatius J (2006). "Lethal congenital contracture syndrome (LCC) and other lethal arthrogryposes in Finland – an epidemiological study". Am. J. Med. Genet. 140A (17): 1834–1839. doi:10.1002/ajmg.a.31381. PMID 16892327. S2CID 23457002.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Norio R (2003). "The Finnish disease heritage III: the individual diseases". Hum. Genet. 112 (5–6): 486–487. doi:10.1007/s00439-002-0877-1. PMID 12627297. S2CID 26741302.
  • Herva R, Leisti J, Kirkinen P, Seppänen U (1985). "A lethal autosomal recessive syndrome of multiple congenital contractures". Am. J. Med. Genet. 20 (3): 431–439. doi:10.1002/ajmg.1320200303. PMID 3993672.
  • Herva R, Conradi N, Kalimo H, Leisti J, Sourander P (1988). "A lethal autosomal recessive syndrome of multiple congenital contractures. Neuropathological analysis of five fetal cases". Am. J. Med. Genet. 29 (1): 67–76. doi:10.1002/ajmg.1320290109. PMID 3344776.
  • Nousiainen HO, Kestilä M, Pakkasjärvi N, Honkala H, Kuure S, Tallila J, Vuopala K, Ignatius J, Herva R, Peltonen L (2008). "Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease". Nature Genetics. 40 (2): 155–157. doi:10.1038/ng.2007.65. PMC 2684619. PMID 18204449.
  • Nousiainen HO, Kestilä M, Pakkasjärvi N, Honkala H, Kuure S, Tallila J, Vuopala K, Ignatius J, Herva R, Peltonen L (February 2008). "Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease". Nature Genetics. 40 (2): 155–157. doi:10.1038/ng.2007.65. PMC 2684619. PMID 18204449.
  • Pakkasjärvi N, Ritvanen A, Herva R, Peltonen L, Kestilä M, Ignatius J (2006). "Lethal congenital contracture syndrome (LCC) and other lethal arthrogryposes in Finland – an epidemiological study". Am. J. Med. Genet. 140A (17): 1834–1839. doi:10.1002/ajmg.a.31381. PMID 16892327. S2CID 23457002.

ncbi.nlm.nih.gov

omim.org

semanticscholar.org

api.semanticscholar.org

  • Norio R (2003). "The Finnish disease heritage III: the individual diseases". Hum. Genet. 112 (5–6): 486–487. doi:10.1007/s00439-002-0877-1. PMID 12627297. S2CID 26741302.
  • Pakkasjärvi N, Ritvanen A, Herva R, Peltonen L, Kestilä M, Ignatius J (2006). "Lethal congenital contracture syndrome (LCC) and other lethal arthrogryposes in Finland – an epidemiological study". Am. J. Med. Genet. 140A (17): 1834–1839. doi:10.1002/ajmg.a.31381. PMID 16892327. S2CID 23457002.