متلازمة كوفين لوري (Arabic Wikipedia)

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

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clsf.info

doi.org

  • Delaunoy JP، Dubos A، Marques Pereira P، Hanauer A (أغسطس 2006). "Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin–Lowry syndrome". Clin. Genet. ج. 70 ع. 2: 161–6. DOI:10.1111/j.1399-0004.2006.00660.x. PMID:16879200.
  • Coffin GS، Siris E، Wegienka LC (1966). "Mental retardation with osteocartilaginous anomalies". Am. J. Dis. Child. ج. 112 ع. 3: 205–213. DOI:10.1001/archpedi.1966.02090120073006.
  • Lowry B، Miller JR، Fraser FC (يونيو 1971). "A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus". Am. J. Dis. Child. ج. 121 ع. 6: 496–500. DOI:10.1001/archpedi.1971.02100170078009. PMID:5581017.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Delaunoy JP، Dubos A، Marques Pereira P، Hanauer A (أغسطس 2006). "Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin–Lowry syndrome". Clin. Genet. ج. 70 ع. 2: 161–6. DOI:10.1111/j.1399-0004.2006.00660.x. PMID:16879200.
  • Lowry B، Miller JR، Fraser FC (يونيو 1971). "A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus". Am. J. Dis. Child. ج. 121 ع. 6: 496–500. DOI:10.1001/archpedi.1971.02100170078009. PMID:5581017.

ninds.nih.gov

rarediseases.org

web.archive.org

whonamedit.com