Murray JC - Search Results

1

Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.

Bureau A, Parker MM, Ruczinski I, Taub MA, Marazita ML, Murray JC, Mangold E, Noethen MM, Ludwig KU, Hetmanski JB, Bailey-Wilson JE, Cropp CD, Li Q, Szymczak S, Albacha-Hejazi H, Alqosayer K, Field LL, Wu-Chou YH, Doheny KF, Ling H, Scott AF, Beaty TH. Bureau A, et al. Among authors: murray jc. Genetics. 2014 Jul;197(3):1039-44. doi: 10.1534/genetics.114.165225. Epub 2014 May 2. Genetics. 2014. PMID: 24793288 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

Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes.

Ferrell RE, Buetow KH, Darby JK, Eichner JE, Murray JC, Smith R, Waziri M, Huson S, Riccardi VM. Ferrell RE, et al. Among authors: murray jc. J Med Genet. 1987 Sep;24(9):522-4. doi: 10.1136/jmg.24.9.522. J Med Genet. 1987. PMID: 3118028 Free PMC article.

6

Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414.

Sander A, Murray JC, Scherpbier-Heddema T, Buetow KH, Weissenbach J, Zingg M, Ludwig K, Schmelzle R. Sander A, et al. Among authors: murray jc. Am J Hum Genet. 1995 Jan;56(1):310-8. Am J Hum Genet. 1995. PMID: 7825592 Free PMC article.

7

Maternal interview reports of family history of birth defects: evaluation from a population-based case-control study of orofacial clefts.

Romitti PA, Burns TL, Murray JC. Romitti PA, et al. Among authors: murray jc. Am J Med Genet. 1997 Nov 12;72(4):422-9. doi: 10.1002/(sici)1096-8628(19971112)72:4<422::aid-ajmg10>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9375725

8

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

9

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.

10

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

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