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EEM syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "EEM syndrome" in English language version.

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

doi.org (Global: 2nd place; English: 2nd place)

  • Hayakawa M, Yanashima K, Kato K, Nakajima A, Yamauchi H (1989). "Association of ectodermal dysplasia, ectrodactyly and macular dystrophy: EEM syndrome (case report)". Ophthalmic Paediatrics and Genetics. 10 (4): 287–292. doi:10.3109/13816818909009884. PMID 2628819.
  • Senecky Y, Halpern GJ, Inbar D, Attias J, Shohat M (2001). "Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblings". American Journal of Medical Genetics. 101 (3): 195–197. doi:10.1002/ajmg.1361. PMID 11424132.
  • Balarin Silva V, Simones AM, Marques-de-Faria AP (1999). "EEM syndrome: report of a family and results of a ten-year follow-up". Ophthalmic Genetics. 20 (2): 95–99. doi:10.1076/opge.20.2.95.2290. PMID 10420194.
  • Kjaer KW, Hansen L, Schwabe GC, Marques-de-Faria AP, Eiberg H, Mundlos S, Tommerup N, Rosenberg T (2005). "Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)". J Med Genet. 42 (4): 292–298. doi:10.1136/jmg.2004.027821. PMC 1736041. PMID 15805154.
  • Shimomura Y, Wajid M, Shapiro L, Christiano AM (2008). "P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle". Development. 135 (4): 743–753. doi:10.1242/dev.006718. PMID 18199584.
  • Zenteno JC, Berdon-Zapata V, Kofman-Alfaro S, Mutchinick O (2005). "Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of Tp63". American Journal of Medical Genetics Part A. 134 (1): 74–76. doi:10.1002/ajmg.a.30277. PMID 15736220. S2CID 38402286.

nih.gov (Global: 4th place; English: 4th place)

pubmed.ncbi.nlm.nih.gov

  • Hayakawa M, Yanashima K, Kato K, Nakajima A, Yamauchi H (1989). "Association of ectodermal dysplasia, ectrodactyly and macular dystrophy: EEM syndrome (case report)". Ophthalmic Paediatrics and Genetics. 10 (4): 287–292. doi:10.3109/13816818909009884. PMID 2628819.
  • Yildirim MS, Ogun TC, Kamis U (2006). "Ectrodactyly, ectodermal dysplasia, macular degeneration syndrome: a further contribution". Genetic Counseling. 17 (2): 149–153. PMID 16970031.
  • Senecky Y, Halpern GJ, Inbar D, Attias J, Shohat M (2001). "Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblings". American Journal of Medical Genetics. 101 (3): 195–197. doi:10.1002/ajmg.1361. PMID 11424132.
  • Balarin Silva V, Simones AM, Marques-de-Faria AP (1999). "EEM syndrome: report of a family and results of a ten-year follow-up". Ophthalmic Genetics. 20 (2): 95–99. doi:10.1076/opge.20.2.95.2290. PMID 10420194.
  • Kjaer KW, Hansen L, Schwabe GC, Marques-de-Faria AP, Eiberg H, Mundlos S, Tommerup N, Rosenberg T (2005). "Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)". J Med Genet. 42 (4): 292–298. doi:10.1136/jmg.2004.027821. PMC 1736041. PMID 15805154.
  • Shimomura Y, Wajid M, Shapiro L, Christiano AM (2008). "P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle". Development. 135 (4): 743–753. doi:10.1242/dev.006718. PMID 18199584.
  • Zenteno JC, Berdon-Zapata V, Kofman-Alfaro S, Mutchinick O (2005). "Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of Tp63". American Journal of Medical Genetics Part A. 134 (1): 74–76. doi:10.1002/ajmg.a.30277. PMID 15736220. S2CID 38402286.

ncbi.nlm.nih.gov

semanticscholar.org (Global: 11th place; English: 8th place)

api.semanticscholar.org

  • Zenteno JC, Berdon-Zapata V, Kofman-Alfaro S, Mutchinick O (2005). "Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of Tp63". American Journal of Medical Genetics Part A. 134 (1): 74–76. doi:10.1002/ajmg.a.30277. PMID 15736220. S2CID 38402286.