Sign In

Login

Password

Forgot Password ? Sign Up

متلازمة بروك (Arabic Wikipedia)

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

refsWebsite
Global rank Arabic rank
8nih.gov
4th place
6th place
6doi.org
2nd place
5th place
1archive.org
6th place
3rd place
1harvard.edu
18th place
33rd place

archive.org

doi.org

  • Mokete، L.؛ Robertson، A.؛ Viljoen، D.؛ Beighton، Peter (2005). "Bruck syndrome: congenital joint contractures with bone fragility". Journal of Orthopaedic Science. ج. 10 ع. 6: 641–646. DOI:10.1007/s00776-005-0958-9. PMID:16307191.
  • Datta، V.؛ Sinha، A.؛ Saili، A.؛ وآخرون (2005). "Osteogenesis Imperfecta". Journal of Pediatrics. ج. 72 ع. 5: 441–442. DOI:10.1007/BF02731745. PMID:15973030.
  • Berg، C.؛ Geipel، A.؛ Noack، F؛ وآخرون (2005). "Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome". Prenatal Diagnosis. ج. 25 ع. 3: 545–548. DOI:10.1002/jbmr.250. PMC:3179293. PMID:20839288.
  • Banks، R.؛ Robins، S.؛ Wijmenga؛ وآخرون (1999). "Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: Indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17". Proceedings of the National Academy of Sciences. ج. 96 ع. 3: 1054–1058. Bibcode:1999PNAS...96.1054B. DOI:10.1073/pnas.96.3.1054. PMC:15349. PMID:9927692.
  • Yapicioglu، H.؛ Ozcan، K.؛ Arikan، O.؛ وآخرون (2009). "Bruck syndrome: osteogenesis imperfecta and arthrogryposis multiplex congenital". Annals of Tropical Paediatrics. ج. 29 ع. 2: 159–1662. DOI:10.1179/146532809x440798. PMID:19460271.
  • Shaheen، Ranad؛ Al-Owain، Mohammed؛ Faqeih، Eissa؛ Al-Hashmi، Nadia؛ Awaji، Ali؛ Al-Zayed، Zayed؛ Alkuraya، Fowzan S (2011). "Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans". American Journal of Medical Genetics Part A. ج. 155 ع. 6: 1448–1452. DOI:10.1002/ajmg.a.34025. PMID:21567934.

harvard.edu

ui.adsabs.harvard.edu

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Mokete، L.؛ Robertson، A.؛ Viljoen، D.؛ Beighton، Peter (2005). "Bruck syndrome: congenital joint contractures with bone fragility". Journal of Orthopaedic Science. ج. 10 ع. 6: 641–646. DOI:10.1007/s00776-005-0958-9. PMID:16307191.
  • Datta، V.؛ Sinha، A.؛ Saili، A.؛ وآخرون (2005). "Osteogenesis Imperfecta". Journal of Pediatrics. ج. 72 ع. 5: 441–442. DOI:10.1007/BF02731745. PMID:15973030.
  • Berg، C.؛ Geipel، A.؛ Noack، F؛ وآخرون (2005). "Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome". Prenatal Diagnosis. ج. 25 ع. 3: 545–548. DOI:10.1002/jbmr.250. PMC:3179293. PMID:20839288.
  • Banks، R.؛ Robins، S.؛ Wijmenga؛ وآخرون (1999). "Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: Indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17". Proceedings of the National Academy of Sciences. ج. 96 ع. 3: 1054–1058. Bibcode:1999PNAS...96.1054B. DOI:10.1073/pnas.96.3.1054. PMC:15349. PMID:9927692.
  • Yapicioglu، H.؛ Ozcan، K.؛ Arikan، O.؛ وآخرون (2009). "Bruck syndrome: osteogenesis imperfecta and arthrogryposis multiplex congenital". Annals of Tropical Paediatrics. ج. 29 ع. 2: 159–1662. DOI:10.1179/146532809x440798. PMID:19460271.
  • Shaheen، Ranad؛ Al-Owain، Mohammed؛ Faqeih، Eissa؛ Al-Hashmi، Nadia؛ Awaji، Ali؛ Al-Zayed، Zayed؛ Alkuraya، Fowzan S (2011). "Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans". American Journal of Medical Genetics Part A. ج. 155 ع. 6: 1448–1452. DOI:10.1002/ajmg.a.34025. PMID:21567934.

ncbi.nlm.nih.gov