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Page 1
Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome.
O'Sullivan J, Bitu CC, Daly SB, Urquhart JE, Barron MJ, Bhaskar SS, Martelli-Júnior H, dos Santos Neto PE, Mansilla MA, Murray JC, Coletta RD, Black GC, Dixon MJ. O'Sullivan J, et al. Among authors: murray jc. Am J Hum Genet. 2011 May 13;88(5):616-20. doi: 10.1016/j.ajhg.2011.04.005. Epub 2011 May 5. Am J Hum Genet. 2011. PMID: 21549343 Free PMC article.
Genetic mapping of the dentinogenesis imperfecta type II locus.
Crosby AH, Scherpbier-Heddema T, Wijmenga C, Altherr MR, Murray JC, Buetow KH, Dixon MJ. Crosby AH, et al. Among authors: murray jc. Am J Hum Genet. 1995 Oct;57(4):832-9. Am J Hum Genet. 1995. PMID: 7573043 Free PMC article.
Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.
Schutte BC, Basart AM, Watanabe Y, Laffin JJ, Coppage K, Bjork BC, Daack-Hirsch S, Patil S, Dixon MJ, Murray JC. Schutte BC, et al. Among authors: murray jc. Am J Med Genet. 1999 May 21;84(2):145-50. doi: 10.1002/(sici)1096-8628(19990521)84:2<145::aid-ajmg11>3.0.co;2-l. Am J Med Genet. 1999. PMID: 10323740
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.
Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, McDonald-McGinn DM, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, Lidral AC, Pober BR, Moreno L, Arcos-Burgos M, Valencia C, Houdayer C, Bahuau M, Moretti-Ferreira D, Richieri-Costa A, Dixon MJ, Murray JC. Kondo S, et al. Among authors: murray jc. Nat Genet. 2002 Oct;32(2):285-9. doi: 10.1038/ng985. Epub 2002 Sep 3. Nat Genet. 2002. PMID: 12219090 Free PMC article.
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.
Marazita ML, Murray JC, Lidral AC, Arcos-Burgos M, Cooper ME, Goldstein T, Maher BS, Daack-Hirsch S, Schultz R, Mansilla MA, Field LL, Liu YE, Prescott N, Malcolm S, Winter R, Ray A, Moreno L, Valencia C, Neiswanger K, Wyszynski DF, Bailey-Wilson JE, Albacha-Hejazi H, Beaty TH, McIntosh I, Hetmanski JB, Tunçbilek G, Edwards M, Harkin L, Scott R, Roddick LG. Marazita ML, et al. Among authors: murray jc. Am J Hum Genet. 2004 Aug;75(2):161-73. doi: 10.1086/422475. Epub 2004 Jun 4. Am J Hum Genet. 2004. PMID: 15185170 Free PMC article.
Contributions of PTCH gene variants to isolated cleft lip and palate.
Mansilla MA, Cooper ME, Goldstein T, Castilla EE, Lopez Camelo JS, Marazita ML, Murray JC. Mansilla MA, et al. Among authors: murray jc. Cleft Palate Craniofac J. 2006 Jan;43(1):21-9. doi: 10.1597/04-169r.1. Cleft Palate Craniofac J. 2006. PMID: 16405370 Free PMC article.
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P.
Choi SJ, Marazita ML, Hart PS, Sulima PP, Field LL, McHenry TG, Govil M, Cooper ME, Letra A, Menezes R, Narayanan S, Mansilla MA, Granjeiro JM, Vieira AR, Lidral AC, Murray JC, Hart TC. Choi SJ, et al. Among authors: murray jc. Eur J Hum Genet. 2009 Jun;17(6):774-84. doi: 10.1038/ejhg.2008.245. Epub 2008 Dec 17. Eur J Hum Genet. 2009. PMID: 19092777 Free PMC article.
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome.
de Lima RL, Hoper SA, Ghassibe M, Cooper ME, Rorick NK, Kondo S, Katz L, Marazita ML, Compton J, Bale S, Hehr U, Dixon MJ, Daack-Hirsch S, Boute O, Bayet B, Revencu N, Verellen-Dumoulin C, Vikkula M, Richieri-Costa A, Moretti-Ferreira D, Murray JC, Schutte BC. de Lima RL, et al. Among authors: murray jc. Genet Med. 2009 Apr;11(4):241-7. doi: 10.1097/GIM.0b013e318197a49a. Genet Med. 2009. PMID: 19282774 Free PMC article.
775 results