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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
Guidelines for the design and analysis of studies on nonsyndromic cleft lip and cleft palate in humans: summary report from a Workshop of the International Consortium for Oral Clefts Genetics.
Mitchell LE, Beaty TH, Lidral AC, Munger RG, Murray JC, Saal HM, Wyszynski DF; International Consortium for Oral Clefts Genetics. Mitchell LE, et al. Among authors: murray jc. Cleft Palate Craniofac J. 2002 Jan;39(1):93-100. doi: 10.1597/1545-1569_2002_039_0093_gftdaa_2.0.co_2. Cleft Palate Craniofac J. 2002. PMID: 11772175
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.
MSX1 and TGFB3 contribute to clefting in South America.
Vieira AR, Orioli IM, Castilla EE, Cooper ME, Marazita ML, Murray JC. Vieira AR, et al. Among authors: murray jc. J Dent Res. 2003 Apr;82(4):289-92. doi: 10.1177/154405910308200409. J Dent Res. 2003. PMID: 12651933
776 results