Murray JC - Search Results

1

IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families.

Leslie EJ, Koboldt DC, Kang CJ, Ma L, Hecht JT, Wehby GL, Christensen K, Czeizel AE, Deleyiannis FW, Fulton RS, Wilson RK, Beaty TH, Schutte BC, Murray JC, Marazita ML. Leslie EJ, et al. Among authors: murray jc. Clin Genet. 2016 Jul;90(1):28-34. doi: 10.1111/cge.12675. Epub 2015 Oct 1. Clin Genet. 2016. PMID: 26346622 Free PMC article.

2

Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4.

Murray JC, Bennett SR, Kwitek AE, Small KW, Schinzel A, Alward WL, Weber JL, Bell GI, Buetow KH. Murray JC, et al. Nat Genet. 1992 Sep;2(1):46-9. doi: 10.1038/ng0992-46. Nat Genet. 1992. PMID: 1303248

3

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.

4

Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate.

Ardinger HH, Buetow KH, Bell GI, Bardach J, VanDemark DR, Murray JC. Ardinger HH, et al. Among authors: murray jc. Am J Hum Genet. 1989 Sep;45(3):348-53. Am J Hum Genet. 1989. PMID: 2570526 Free PMC article.

5

Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41.

Schutte BC, Sander A, Malik M, Murray JC. Schutte BC, et al. Among authors: murray jc. Genomics. 1996 Sep 15;36(3):507-14. doi: 10.1006/geno.1996.0496. Genomics. 1996. PMID: 8884274

6

Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locus.

Peiffer-Schneider S, Schutte BC, Murray JC, Frees KL, Williamson K, Leysens NJ, Schwartz DA. Peiffer-Schneider S, et al. Among authors: murray jc. Mamm Genome. 1997 Oct;8(10):785-6. doi: 10.1007/s003359900569. Mamm Genome. 1997. PMID: 9321479 No abstract available.

7

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

8

Oral clefts, transforming growth factor alpha gene variants, and maternal smoking: a population-based case-control study in Denmark, 1991-1994.

Christensen K, Olsen J, Nørgaard-Pedersen B, Basso O, Støvring H, Milhollin-Johnson L, Murray JC. Christensen K, et al. Among authors: murray jc. Am J Epidemiol. 1999 Feb 1;149(3):248-55. doi: 10.1093/oxfordjournals.aje.a009799. Am J Epidemiol. 1999. PMID: 9927220

9

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

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

775 results

Search Page

Filters