Crouzon syndrome (English Wikipedia)

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

refsWebsite

Global rank English rank

4^th place

2^nd place

2,888^th place

2,730^th place

610^th place

704^th place

5,181^st place

3,260^th place

18^th place

17^th place

doi.org

Gray, Thomas L.; Casey, Theresa; Selva, Dinesh; Anderson, Peter J.; David, David J. (9 May 2005). "Ophthalmic Sequelae of Crouzon Syndrome". Ophthalmology. 112 (6): 1129–1134. doi:10.1016/j.ophtha.2004.12.037. PMID 15885794.
Snyder-Warwick AK, Perlyn CA, Pan J, Yu K, Zhang L, Ornitz DM (February 2010). "Analysis of a gain-of-function FGFR2 Crouzon mutation provides evidence of loss of function activity in the etiology of cleft palate". Proc. Natl. Acad. Sci. U.S.A. 107 (6): 2515–20. Bibcode:2010PNAS..107.2515S. doi:10.1073/pnas.0913985107. PMC 2823872. PMID 20133659.
Fenwick AL, Goos JA, Rankin J, Lord H, Lester T, Hoogeboom AJ, van den Ouweland AM, Wall SA, Mathijssen IM, Wilkie AO (August 2014). "Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndrome". BMC Med. Genet. 15: 95. doi:10.1186/s12881-014-0095-4. PMC 4236556. PMID 25174698.
Di Rocco F, Biosse Duplan M, Heuzé Y, Kaci N, Komla-Ebri D, Munnich A, Mugniery E, Benoist-Lasselin C, Legeai-Mallet L (June 2014). "FGFR3 mutation causes abnormal membranous ossification in achondroplasia". Hum. Mol. Genet. 23 (11): 2914–25. doi:10.1093/hmg/ddu004. PMID 24419316.

Gray, Thomas L.; Casey, Theresa; Selva, Dinesh; Anderson, Peter J.; David, David J. (9 May 2005). "Ophthalmic Sequelae of Crouzon Syndrome". Ophthalmology. 112 (6): 1129–1134. doi:10.1016/j.ophtha.2004.12.037. PMID 15885794.

Gray, Thomas L.; Casey, Theresa; Selva, Dinesh; Anderson, Peter J.; David, David J. (9 May 2005). "Ophthalmic Sequelae of Crouzon Syndrome". Ophthalmology. 112 (6): 1129–1134. doi:10.1016/j.ophtha.2004.12.037. PMID 15885794.
Snyder-Warwick AK, Perlyn CA, Pan J, Yu K, Zhang L, Ornitz DM (February 2010). "Analysis of a gain-of-function FGFR2 Crouzon mutation provides evidence of loss of function activity in the etiology of cleft palate". Proc. Natl. Acad. Sci. U.S.A. 107 (6): 2515–20. Bibcode:2010PNAS..107.2515S. doi:10.1073/pnas.0913985107. PMC 2823872. PMID 20133659.
Fenwick AL, Goos JA, Rankin J, Lord H, Lester T, Hoogeboom AJ, van den Ouweland AM, Wall SA, Mathijssen IM, Wilkie AO (August 2014). "Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndrome". BMC Med. Genet. 15: 95. doi:10.1186/s12881-014-0095-4. PMC 4236556. PMID 25174698.
Di Rocco F, Biosse Duplan M, Heuzé Y, Kaci N, Komla-Ebri D, Munnich A, Mugniery E, Benoist-Lasselin C, Legeai-Mallet L (June 2014). "FGFR3 mutation causes abnormal membranous ossification in achondroplasia". Hum. Mol. Genet. 23 (11): 2914–25. doi:10.1093/hmg/ddu004. PMID 24419316.
Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LH, Stephens K, Amemiya A, Robin NH, Falk MJ, Haldeman-Englert CR (October 20, 1998). "FGFR-Related Craniosynostosis Syndromes". GeneReviews. PMID 20301628.

"Crouzon syndrome". rarediseases.info.nih.gov. US: Genetic and Rare Diseases Information Center (GARD), National Institutes of Health. Retrieved 21 November 2018.

"Crouzon syndrome". Genetics Home Reference. US: US National Library of Medicine, National Institutes of Health. Retrieved 21 November 2018 – via ghr.nlm.nih.gov.