Синдром Тричера Коллінза (Ukrainian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Синдром Тричера Коллінза" in Ukrainian language version.

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9nih.gov

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7doi.org

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6wikidata.org

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4wikipedia.org

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2worldcat.org

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2clinicalgenome.org

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2web.archive.org

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1opentargets.org

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1obolibrary.org

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1ngmu.ru

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clinicalgenome.org

search.clinicalgenome.org

doi.org

dx.doi.org

Dixon M. J. Treacher Collins syndrome // Human Molecular Genetics — OUP, 1996. — Vol. 5 Spec No. — P. 1391–6. — ISSN 0964-6906; 1460-2083 — doi:10.1093/HMG/5.SUPPLEMENT_1.1391
d:Track:Q217595 d:Track:Q2720965 d:Track:Q55670362
Zweier C., Hoefsloot L. H. Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome // Nature Genetics / M. Axton, T. Faial — NPG, 2010. — Vol. 43, Iss. 1. — P. 20–22. — ISSN 1061-4036; 1546-1718 — doi:10.1038/NG.724
d:Track:Q34153403 d:Track:Q37631205 d:Track:Q976454 d:Track:Q180419 d:Track:Q113000985 d:Track:Q47528456 d:Track:Q56753445
Chiara Conte, Maria Rosaria D'Apice, Fabrizio Rinaldi, Stefano Gambardella, Federica Sangiuolo and Giuseppe Novelli. Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome // BMC Med Genet. : journal. — 2011. — Vol. 12, (9). — DOI:10.1186/1471-2350-12-125. — PMID 21951868 .
Dixon M.J., Dixon J., Raskova D., et al. Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2 // Human Molecular Genetics^[en] : journal. — Oxford University Press, 1993. — Vol. 1, no. 4 (8 May). — P. 249—253. — DOI:10.1093/hmg/1.4.249. — PMID 1303194 .
Evans, Adele Karen; Rahbar, Reza; Rogers, Gary F.; Mulliken, John B.; Volk, Mark S. Robin sequence: A retrospective review of 115 patients // International Journal of Pediatric Otorhinolaryngology : journal. — 2006. — Vol. 70, no. 6, (5). — P. 973—980. — DOI:10.1016/j.ijporl.2005.10.016. — PMID 16443284 .
Argenta, Louis C.; Iacobucci, John J. Treacher Collins Syndrome: Present concepts of the disorder and their surgical correction // World Journal of Surgery : journal. — 1989. — Vol. 13, no. 4, (6). — P. 401—409. — DOI:10.1007/BF01660753. — PMID 2773500 .
Marres, H.A. Hearing loss in the Treacher-Collins syndrome // Advances in oto-rhino-laryngology. — 2002. — Т. 61 (8 May). — С. 209—215. — DOI:10.1159/000066811. — PMID 12408086 .

ngmu.ru

Электронный научный журнал «Медицина и образование в Сибири». Архів оригіналу за 2 квітня 2015. Процитовано 22 жовтня 2010.

nih.gov

ncbi.nlm.nih.gov

Chiara Conte, Maria Rosaria D'Apice, Fabrizio Rinaldi, Stefano Gambardella, Federica Sangiuolo and Giuseppe Novelli. Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome // BMC Med Genet. : journal. — 2011. — Vol. 12, (9). — DOI:10.1186/1471-2350-12-125. — PMID 21951868 .
Dixon M.J., Dixon J., Raskova D., et al. Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2 // Human Molecular Genetics^[en] : journal. — Oxford University Press, 1993. — Vol. 1, no. 4 (8 May). — P. 249—253. — DOI:10.1093/hmg/1.4.249. — PMID 1303194 .
Dixon M.J., Dixon J., Houseal T., et al. Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1 // American Journal of Human Genetics^[en] : journal. — 1993. — Vol. 52, no. 5 (8 May). — P. 907—914. — PMID 8488840 .
Goel L., Bennur S.K., Jambhale S. Treacher Collins syndrome-a challenge for anaesthesiologists // Indian Journal of Anaesthesia^[en] : journal. — 2009. — Vol. 53, no. 4 (8). — P. 496—500. — PMID 20640217 .
Evans, Adele Karen; Rahbar, Reza; Rogers, Gary F.; Mulliken, John B.; Volk, Mark S. Robin sequence: A retrospective review of 115 patients // International Journal of Pediatric Otorhinolaryngology : journal. — 2006. — Vol. 70, no. 6, (5). — P. 973—980. — DOI:10.1016/j.ijporl.2005.10.016. — PMID 16443284 .
Argenta, Louis C.; Iacobucci, John J. Treacher Collins Syndrome: Present concepts of the disorder and their surgical correction // World Journal of Surgery : journal. — 1989. — Vol. 13, no. 4, (6). — P. 401—409. — DOI:10.1007/BF01660753. — PMID 2773500 .
Marres, HA; Cremers, CW; Marres, E.H. Treacher-Collins syndrome. Management of major and minor anomalies of the ear // Revue de laryngologie - otologie - rhinologie : journal. — 1995. — Vol. 116, no. 2 (8 May). — P. 105—108. — PMID 7569369 .
Marres, H.A. Hearing loss in the Treacher-Collins syndrome // Advances in oto-rhino-laryngology. — 2002. — Т. 61 (8 May). — С. 209—215. — DOI:10.1159/000066811. — PMID 12408086 .

ghr.nlm.nih.gov

Treacher Collins syndrome. Genetics Home Reference (англ.). June 2012. Архів оригіналу за 26 червня 2020. Процитовано 22 липня 2020.

obolibrary.org

purl.obolibrary.org

Disease Ontology — 2016.
d:Track:Q4117183 d:Track:Q5282129

opentargets.org

platform.opentargets.org

Open Targets Platform
d:Track:Q107517929 d:Track:Q113138000

web.archive.org

Treacher Collins syndrome. Genetics Home Reference (англ.). June 2012. Архів оригіналу за 26 червня 2020. Процитовано 22 липня 2020.
Электронный научный журнал «Медицина и образование в Сибири». Архів оригіналу за 2 квітня 2015. Процитовано 22 жовтня 2010.

wikidata.org

Dixon M. J. Treacher Collins syndrome // Human Molecular Genetics — OUP, 1996. — Vol. 5 Spec No. — P. 1391–6. — ISSN 0964-6906; 1460-2083 — doi:10.1093/HMG/5.SUPPLEMENT_1.1391
d:Track:Q217595 d:Track:Q2720965 d:Track:Q55670362
ClinGen
d:Track:Q64403342
ClinGen
d:Track:Q64403342
Zweier C., Hoefsloot L. H. Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome // Nature Genetics / M. Axton, T. Faial — NPG, 2010. — Vol. 43, Iss. 1. — P. 20–22. — ISSN 1061-4036; 1546-1718 — doi:10.1038/NG.724
d:Track:Q34153403 d:Track:Q37631205 d:Track:Q976454 d:Track:Q180419 d:Track:Q113000985 d:Track:Q47528456 d:Track:Q56753445
Open Targets Platform
d:Track:Q107517929 d:Track:Q113138000
Disease Ontology — 2016.
d:Track:Q4117183 d:Track:Q5282129

wikipedia.org

en.wikipedia.org

Dixon M. J. Treacher Collins syndrome // Human Molecular Genetics — OUP, 1996. — Vol. 5 Spec No. — P. 1391–6. — ISSN 0964-6906; 1460-2083 — doi:10.1093/HMG/5.SUPPLEMENT_1.1391
d:Track:Q217595 d:Track:Q2720965 d:Track:Q55670362
Dixon M.J., Dixon J., Raskova D., et al. Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2 // Human Molecular Genetics^[en] : journal. — Oxford University Press, 1993. — Vol. 1, no. 4 (8 May). — P. 249—253. — DOI:10.1093/hmg/1.4.249. — PMID 1303194 .
Dixon M.J., Dixon J., Houseal T., et al. Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1 // American Journal of Human Genetics^[en] : journal. — 1993. — Vol. 52, no. 5 (8 May). — P. 907—914. — PMID 8488840 .
Goel L., Bennur S.K., Jambhale S. Treacher Collins syndrome-a challenge for anaesthesiologists // Indian Journal of Anaesthesia^[en] : journal. — 2009. — Vol. 53, no. 4 (8). — P. 496—500. — PMID 20640217 .

worldcat.org

Dixon M. J. Treacher Collins syndrome // Human Molecular Genetics — OUP, 1996. — Vol. 5 Spec No. — P. 1391–6. — ISSN 0964-6906; 1460-2083 — doi:10.1093/HMG/5.SUPPLEMENT_1.1391
d:Track:Q217595 d:Track:Q2720965 d:Track:Q55670362
Zweier C., Hoefsloot L. H. Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome // Nature Genetics / M. Axton, T. Faial — NPG, 2010. — Vol. 43, Iss. 1. — P. 20–22. — ISSN 1061-4036; 1546-1718 — doi:10.1038/NG.724
d:Track:Q34153403 d:Track:Q37631205 d:Track:Q976454 d:Track:Q180419 d:Track:Q113000985 d:Track:Q47528456 d:Track:Q56753445