Murray JC - Search Results

1

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

2

Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq.

Murray JC, Nishimura DY, Buetow KH, Ardinger HH, Spence MA, Sparkes RS, Falk RE, Falk PM, Gardner RJ, Harkness EM, et al. Murray JC, et al. Am J Hum Genet. 1990 Mar;46(3):486-91. Am J Hum Genet. 1990. PMID: 2309700 Free PMC article.

3

Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines.

Lidral AC, Murray JC, Buetow KH, Basart AM, Schearer H, Shiang R, Naval A, Layda E, Magee K, Magee W. Lidral AC, et al. Among authors: murray jc. Cleft Palate Craniofac J. 1997 Jan;34(1):1-6. doi: 10.1597/1545-1569_1997_034_0001_sotcgt_2.3.co_2. Cleft Palate Craniofac J. 1997. PMID: 9003904

4

Clinical and epidemiologic studies of cleft lip and palate in the Philippines.

Murray JC, Daack-Hirsch S, Buetow KH, Munger R, Espina L, Paglinawan N, Villanueva E, Rary J, Magee K, Magee W. Murray JC, et al. Cleft Palate Craniofac J. 1997 Jan;34(1):7-10. doi: 10.1597/1545-1569_1997_034_0007_caesoc_2.3.co_2. Cleft Palate Craniofac J. 1997. PMID: 9003905

5

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.

Lidral AC, Romitti PA, Basart AM, Doetschman T, Leysens NJ, Daack-Hirsch S, Semina EV, Johnson LR, Machida J, Burds A, Parnell TJ, Rubenstein JL, Murray JC. Lidral AC, et al. Among authors: murray jc. Am J Hum Genet. 1998 Aug;63(2):557-68. doi: 10.1086/301956. Am J Hum Genet. 1998. PMID: 9683588 Free PMC article.

6

Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate.

Yoshiura K, Machida J, Daack-Hirsch S, Patil SR, Ashworth LK, Hecht JT, Murray JC. Yoshiura K, et al. Among authors: murray jc. Genomics. 1998 Dec 1;54(2):231-40. doi: 10.1006/geno.1998.5577. Genomics. 1998. PMID: 9828125

7

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

8

The many faces and factors of orofacial clefts.

Schutte BC, Murray JC. Schutte BC, et al. Among authors: murray jc. Hum Mol Genet. 1999;8(10):1853-9. doi: 10.1093/hmg/8.10.1853. Hum Mol Genet. 1999. PMID: 10469837 Review.

9

Transforming growth factor-alpha (TGFA): genomic structure, boundary sequences, and mutation analysis in nonsyndromic cleft lip/palate and cleft palate only.

Machida J, Yoshiura Ki, Funkhauser CD, Natsume N, Kawai T, Murray JC. Machida J, et al. Among authors: murray jc. Genomics. 1999 Nov 1;61(3):237-42. doi: 10.1006/geno.1999.5962. Genomics. 1999. PMID: 10552925

10

A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.

Schutte BC, Bjork BC, Coppage KB, Malik MI, Gregory SG, Scott DJ, Brentzell LM, Watanabe Y, Dixon MJ, Murray JC. Schutte BC, et al. Among authors: murray jc. Genome Res. 2000 Jan;10(1):81-94. Genome Res. 2000. PMID: 10645953 Free PMC article.

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