الاختلافات الجسدية البشرية (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "الاختلافات الجسدية البشرية" in Arabic language version.

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archive.org

cell.com

doi.org

  • Li، Chun؛ Williams، Scott M. (1 ديسمبر 2013). "Human Somatic Variation: It's Not Just for Cancer Anymore". Current Genetic Medicine Reports. ج. 1 ع. 4: 212–218. DOI:10.1007/s40142-013-0029-z. ISSN:2167-4876.
  • Youssoufian، Hagop؛ Pyeritz، Reed E. (أكتوبر 2002). "Mechanisms and consequences of somatic mosaicism in humans". Nature Reviews Genetics. ج. 3 ع. 10: 748–758. DOI:10.1038/nrg906. ISSN:1471-0064. PMID:12360233. S2CID:6355589.
  • De, Subhajyoti (1 Jun 2011). "Somatic mosaicism in healthy human tissues". Trends in Genetics (بالإنجليزية). 27 (6): 217–223. DOI:10.1016/j.tig.2011.03.002. ISSN:0168-9525. PMID:21496937. Archived from the original on 2013-10-15.
  • Vanneste، Evelyne؛ Voet، Thierry؛ Le Caignec، Cédric؛ Ampe، Michèle؛ Konings، Peter؛ Melotte، Cindy؛ Debrock، Sophie؛ Amyere، Mustapha؛ Vikkula، Miikka؛ Schuit، Frans؛ Fryns، Jean-Pierre (مايو 2002). "Chromosome instability is common in human cleavage-stage embryos". Nature Medicine. ج. 15 ع. 5: 577–583. DOI:10.1038/nm.1924. ISSN:1546-170X. PMID:19396175. S2CID:10530085.
  • Kalousek، D. K.؛ Dill، F. J. (12 أغسطس 1983). "Chromosomal mosaicism confined to the placenta in human conceptions". Science. ج. 221 ع. 4611: 665–667. Bibcode:1983Sci...221..665K. DOI:10.1126/science.6867735. ISSN:0036-8075. PMID:6867735.
  • Leach، Natalia T.؛ Rehder، Catherine؛ Jensen، Keith؛ Holt، Shawn؛ Jackson-Cook، Colleen (1 أغسطس 2004). "Human chromosomes with shorter telomeres and large heterochromatin regions have a higher frequency of acquired somatic cell aneuploidy". Mechanisms of Ageing and Development. ج. 125 ع. 8: 563–573. DOI:10.1016/j.mad.2004.06.006. ISSN:0047-6374. PMID:15336914. S2CID:19899116.
  • Bruder، Carl E. G.؛ Piotrowski، Arkadiusz؛ Gijsbers، Antoinet A. C. J.؛ Andersson، Robin؛ Erickson، Stephen؛ Diaz de Ståhl، Teresita؛ Menzel، Uwe؛ Sandgren، Johanna؛ von Tell، Desiree؛ Poplawski، Andrzej؛ Crowley، Michael (3 مارس 2008). "Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles". The American Journal of Human Genetics. ج. 82 ع. 3: 763–771. DOI:10.1016/j.ajhg.2007.12.011. ISSN:0002-9297. PMC:2427204. PMID:18304490.
  • Halaschek-Wiener، Julius؛ Vulto، Irma؛ Fornika، Dan؛ Collins، Jennifer؛ Connors، Joseph M.؛ Le، Nhu D.؛ Lansdorp، Peter M.؛ Brooks-Wilson، Angela (1 نوفمبر 2008). "Reduced telomere length variation in healthy oldest old". Mechanisms of Ageing and Development. ج. 129 ع. 11: 638–641. DOI:10.1016/j.mad.2008.07.004. ISSN:0047-6374. PMID:18765247. S2CID:2595117.

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ui.adsabs.harvard.edu

kuleuven.be

lirias.kuleuven.be

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

web.archive.org

worldcat.org

  • Li، Chun؛ Williams، Scott M. (1 ديسمبر 2013). "Human Somatic Variation: It's Not Just for Cancer Anymore". Current Genetic Medicine Reports. ج. 1 ع. 4: 212–218. DOI:10.1007/s40142-013-0029-z. ISSN:2167-4876.
  • Youssoufian، Hagop؛ Pyeritz، Reed E. (أكتوبر 2002). "Mechanisms and consequences of somatic mosaicism in humans". Nature Reviews Genetics. ج. 3 ع. 10: 748–758. DOI:10.1038/nrg906. ISSN:1471-0064. PMID:12360233. S2CID:6355589.
  • De, Subhajyoti (1 Jun 2011). "Somatic mosaicism in healthy human tissues". Trends in Genetics (بالإنجليزية). 27 (6): 217–223. DOI:10.1016/j.tig.2011.03.002. ISSN:0168-9525. PMID:21496937. Archived from the original on 2013-10-15.
  • Vanneste، Evelyne؛ Voet، Thierry؛ Le Caignec، Cédric؛ Ampe، Michèle؛ Konings، Peter؛ Melotte، Cindy؛ Debrock، Sophie؛ Amyere، Mustapha؛ Vikkula، Miikka؛ Schuit، Frans؛ Fryns، Jean-Pierre (مايو 2002). "Chromosome instability is common in human cleavage-stage embryos". Nature Medicine. ج. 15 ع. 5: 577–583. DOI:10.1038/nm.1924. ISSN:1546-170X. PMID:19396175. S2CID:10530085.
  • Kalousek، D. K.؛ Dill، F. J. (12 أغسطس 1983). "Chromosomal mosaicism confined to the placenta in human conceptions". Science. ج. 221 ع. 4611: 665–667. Bibcode:1983Sci...221..665K. DOI:10.1126/science.6867735. ISSN:0036-8075. PMID:6867735.
  • Leach، Natalia T.؛ Rehder، Catherine؛ Jensen، Keith؛ Holt، Shawn؛ Jackson-Cook، Colleen (1 أغسطس 2004). "Human chromosomes with shorter telomeres and large heterochromatin regions have a higher frequency of acquired somatic cell aneuploidy". Mechanisms of Ageing and Development. ج. 125 ع. 8: 563–573. DOI:10.1016/j.mad.2004.06.006. ISSN:0047-6374. PMID:15336914. S2CID:19899116.
  • Bruder، Carl E. G.؛ Piotrowski، Arkadiusz؛ Gijsbers، Antoinet A. C. J.؛ Andersson، Robin؛ Erickson، Stephen؛ Diaz de Ståhl، Teresita؛ Menzel، Uwe؛ Sandgren، Johanna؛ von Tell، Desiree؛ Poplawski، Andrzej؛ Crowley، Michael (3 مارس 2008). "Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles". The American Journal of Human Genetics. ج. 82 ع. 3: 763–771. DOI:10.1016/j.ajhg.2007.12.011. ISSN:0002-9297. PMC:2427204. PMID:18304490.
  • Halaschek-Wiener، Julius؛ Vulto، Irma؛ Fornika، Dan؛ Collins، Jennifer؛ Connors، Joseph M.؛ Le، Nhu D.؛ Lansdorp، Peter M.؛ Brooks-Wilson، Angela (1 نوفمبر 2008). "Reduced telomere length variation in healthy oldest old". Mechanisms of Ageing and Development. ج. 129 ع. 11: 638–641. DOI:10.1016/j.mad.2008.07.004. ISSN:0047-6374. PMID:18765247. S2CID:2595117.
  • Ellis، N A؛ Lennon، D J؛ Proytcheva، M؛ Alhadeff، B؛ Henderson، E E؛ German، J (نوفمبر 1995). "Somatic intragenic recombination within the mutated locus BLM can correct the high sister-chromatid exchange phenotype of Bloom syndrome cells". American Journal of Human Genetics. ج. 57 ع. 5: 1019–1027. ISSN:0002-9297. PMC:1801389. PMID:7485150.