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SATB2 (Catalan Wikipedia)

Analysis of information sources in references of the Wikipedia article "SATB2" in Catalan language version.

refsWebsite
Global rank Catalan rank
9nih.gov
4th place
7th place
6doi.org
2nd place
6th place
2ensembl.org
1,626th place
8,169th place
1wikidata.org
43rd place
170th place

doi.org

dx.doi.org

  • Kikuno R, Nagase T, Ishikawa K, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O «Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro». DNA Res., 6, 3, Juny 1999, pàg. 197–205. DOI: 10.1093/dnares/6.3.197. PMID: 10470851.
  • Rosenfeld JA, Ballif BC, Lucas A, et al. «Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome.». PLoS ONE, 4, 8, 2009, pàg. e6568. DOI: 10.1371/journal.pone.0006568. PMID: 19668335.
  • Jugessur A, Shi M, Gjessing HK, et al. «Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.». PLoS ONE, 5, 7, 2010, pàg. e11493. DOI: 10.1371/journal.pone.0011493. PMC: 2901336. PMID: 20634891.
  • Beaty TH, Hetmanski JB, Fallin MD, et al. «Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations.». Hum. Genet., 120, 4, 2006, pàg. 501–18. DOI: 10.1007/s00439-006-0235-9. PMID: 16953426.
  • Dixon MJ, Marazita ML, Beaty TH, Murray JC «Cleft lip and palate: understanding genetic and environmental influences». Nat. Rev. Genet., 12, 3, Març 2011, pàg. 167–78. DOI: 10.1038/nrg2933. PMC: 3086810. PMID: 21331089.
  • FitzPatrick DR, Carr IM, McLaren L, Leek JP, Wightman P, Williamson K, Gautier P, McGill N, Hayward C, Firth H, Markham AF, Fantes JA, Bonthron DT «Identification of SATB2 as the cleft palate gene on 2q32-q33». Hum. Mol. Genet., 12, 19, Octubre 2003, pàg. 2491–501. DOI: 10.1093/hmg/ddg248. PMID: 12915443.

ensembl.org

May2017.archive.ensembl.org

nih.gov

ncbi.nlm.nih.gov

  • «Human PubMed Reference:». National Center for Biotechnology Information, U.S. National Library of Medicine.
  • «Mouse PubMed Reference:». National Center for Biotechnology Information, U.S. National Library of Medicine.
  • Kikuno R, Nagase T, Ishikawa K, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O «Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro». DNA Res., 6, 3, Juny 1999, pàg. 197–205. DOI: 10.1093/dnares/6.3.197. PMID: 10470851.
  • «Entrez Gene: SATB homeobox 2».
  • Rosenfeld JA, Ballif BC, Lucas A, et al. «Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome.». PLoS ONE, 4, 8, 2009, pàg. e6568. DOI: 10.1371/journal.pone.0006568. PMID: 19668335.
  • Jugessur A, Shi M, Gjessing HK, et al. «Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.». PLoS ONE, 5, 7, 2010, pàg. e11493. DOI: 10.1371/journal.pone.0011493. PMC: 2901336. PMID: 20634891.
  • Beaty TH, Hetmanski JB, Fallin MD, et al. «Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations.». Hum. Genet., 120, 4, 2006, pàg. 501–18. DOI: 10.1007/s00439-006-0235-9. PMID: 16953426.
  • Dixon MJ, Marazita ML, Beaty TH, Murray JC «Cleft lip and palate: understanding genetic and environmental influences». Nat. Rev. Genet., 12, 3, Març 2011, pàg. 167–78. DOI: 10.1038/nrg2933. PMC: 3086810. PMID: 21331089.
  • FitzPatrick DR, Carr IM, McLaren L, Leek JP, Wightman P, Williamson K, Gautier P, McGill N, Hayward C, Firth H, Markham AF, Fantes JA, Bonthron DT «Identification of SATB2 as the cleft palate gene on 2q32-q33». Hum. Mol. Genet., 12, 19, Octubre 2003, pàg. 2491–501. DOI: 10.1093/hmg/ddg248. PMID: 12915443.

wikidata.org