Síndrome de Coffin-Siris (Catalan Wikipedia)

Analysis of information sources in references of the Wikipedia article "Síndrome de Coffin-Siris" in Catalan language version.

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archive.org

«Coffin-Siris syndrome». Journal of Medical Genetics, 28, 5, 5-1991, pàg. 338–41. DOI: 10.1136/jmg.28.5.338. PMC: 1016855. PMID: 1865473.

doi.org

dx.doi.org

«Coffin-Siris syndrome». Journal of Medical Genetics, 28, 5, 5-1991, pàg. 338–41. DOI: 10.1136/jmg.28.5.338. PMC: 1016855. PMID: 1865473.
«Nicolaides-Baraitser syndrome: Delineation of the phenotype». American Journal of Medical Genetics. Part A, 149A, 8, 8-2009, pàg. 1628–40. DOI: 10.1002/ajmg.a.32956. PMID: 19606471.
«Coffin-Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene». European Journal of Human Genetics, 22, 11, 11-2014, pàg. 1327–9. DOI: 10.1038/ejhg.2014.25. PMC: 4200437. PMID: 24569609.
«De novo SOX11 mutations cause Coffin-Siris syndrome». Nature Communications, 5, 6-2014, pàg. 4011. Bibcode: 2014NatCo...5.4011T. DOI: 10.1038/ncomms5011. PMID: 24886874.
«Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients». European Journal of Medical Genetics, 62, 1, 4-2018, pàg. 27–34. DOI: 10.1016/j.ejmg.2018.04.014. PMID: 29698805.

gla.ac.uk

eprints.gla.ac.uk

«Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients». European Journal of Medical Genetics, 62, 1, 4-2018, pàg. 27–34. DOI: 10.1016/j.ejmg.2018.04.014. PMID: 29698805.

harvard.edu

adsabs.harvard.edu

«De novo SOX11 mutations cause Coffin-Siris syndrome». Nature Communications, 5, 6-2014, pàg. 4011. Bibcode: 2014NatCo...5.4011T. DOI: 10.1038/ncomms5011. PMID: 24886874.

ledgertranscript.com

«Greenville: A home of one's own - Ledger Transcript». Ledger Transcript, 14-05-2015.

metro.co.uk

metrowebukmetro. «Twisted spine girl back playing football». Metro, 13-10-2008.

nih.gov

ncbi.nlm.nih.gov

«Coffin-Siris syndrome». Journal of Medical Genetics, 28, 5, 5-1991, pàg. 338–41. DOI: 10.1136/jmg.28.5.338. PMC: 1016855. PMID: 1865473.
«Nicolaides-Baraitser syndrome: Delineation of the phenotype». American Journal of Medical Genetics. Part A, 149A, 8, 8-2009, pàg. 1628–40. DOI: 10.1002/ajmg.a.32956. PMID: 19606471.
«Coffin-Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene». European Journal of Human Genetics, 22, 11, 11-2014, pàg. 1327–9. DOI: 10.1038/ejhg.2014.25. PMC: 4200437. PMID: 24569609.
«De novo SOX11 mutations cause Coffin-Siris syndrome». Nature Communications, 5, 6-2014, pàg. 4011. Bibcode: 2014NatCo...5.4011T. DOI: 10.1038/ncomms5011. PMID: 24886874.
«Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients». European Journal of Medical Genetics, 62, 1, 4-2018, pàg. 27–34. DOI: 10.1016/j.ejmg.2018.04.014. PMID: 29698805.

ghr.nlm.nih.gov

«Coffin-Siris syndrome». Genetics Home Reference, 08-06-2015.

washingtonpost.com

Cha, Ariana Eunjung. «NIH researchers sequence healthy volunteers' DNA and find they aren't so healthy after all». Washington Post, 04-06-2015.