Sign In

Login

Password

Forgot Password ? Sign Up

متلازمة كوهين (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "متلازمة كوهين" in Arabic language version.

refsWebsite
Global rank Arabic rank
4nih.gov
4th place
6th place
2doi.org
2nd place
5th place

doi.org

  • Kolehmainen J، Black GC، Saarinen A، وآخرون (2003). "Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport". Am. J. Hum. Genet. ج. 72 ع. 6: 1359–69. DOI:10.1086/375454. PMC:1180298. PMID:12730828.
  • Norio، R؛ Raitta، C (1986). "Are the Mirhosseini-Holmes-Walton syndrome and the Cohen syndrome identical?". Am. J. Med. Genet. ج. 25 ع. 2: 397–8. DOI:10.1002/ajmg.1320250227. PMID:3096139.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Kolehmainen J، Black GC، Saarinen A، وآخرون (2003). "Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport". Am. J. Hum. Genet. ج. 72 ع. 6: 1359–69. DOI:10.1086/375454. PMC:1180298. PMID:12730828.
  • Horn D، Krebsová A، Kunze J، Reis A (2000). "Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3-8q22.1: redefining a clinical entity". American Journal of Medical Genetics. ج. 92 ع. 4: 285–92. PMID:10842298.
  • Norio، R؛ Raitta، C (1986). "Are the Mirhosseini-Holmes-Walton syndrome and the Cohen syndrome identical?". Am. J. Med. Genet. ج. 25 ع. 2: 397–8. DOI:10.1002/ajmg.1320250227. PMID:3096139.

ncbi.nlm.nih.gov

  • Kolehmainen J، Black GC، Saarinen A، وآخرون (2003). "Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport". Am. J. Hum. Genet. ج. 72 ع. 6: 1359–69. DOI:10.1086/375454. PMC:1180298. PMID:12730828.