Murray JC - Search Results

1

Face facts: genes, environment, and clefts.

Murray JC. Murray JC. Am J Hum Genet. 1995 Aug;57(2):227-32. Am J Hum Genet. 1995. PMID: 7668246 Free PMC article. No abstract available.

2

Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome.

Sander A, Schmelzle R, Murray J. Sander A, et al. Hum Mol Genet. 1994 Apr;3(4):575-8. doi: 10.1093/hmg/3.4.575. Hum Mol Genet. 1994. PMID: 8069301

3

Dentin phosphoprotein gene locus is not associated with dentinogenesis imperfecta types II and III.

MacDougall M, Zeichner-David M, Murray J, Crall M, Davis A, Slavkin H. MacDougall M, et al. Am J Hum Genet. 1992 Jan;50(1):190-4. Am J Hum Genet. 1992. PMID: 1729887 Free PMC article.

4

Time for T.

Murray JC. Murray JC. Nat Genet. 2001 Oct;29(2):107-9. doi: 10.1038/ng1001-107. Nat Genet. 2001. PMID: 11586288

5

A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3.

Sertié AL, Quimby M, Moreira ES, Murray J, Zatz M, Antonarakis SE, Passos-Bueno MR. Sertié AL, et al. Hum Mol Genet. 1996 Jun;5(6):843-7. doi: 10.1093/hmg/5.6.843. Hum Mol Genet. 1996. PMID: 8776601

6

Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome.

Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. Suzuki OT, et al. Am J Hum Genet. 2002 Dec;71(6):1320-9. doi: 10.1086/344695. Epub 2002 Nov 1. Am J Hum Genet. 2002. PMID: 12415512 Free PMC article.

7

The Bell Curve: statement by the NIH-DOE Joint Working Group on the Ethical, Legal, and Social Implications of Human Genome Research.

Allen A, Anderson B, Andrews L, Beckwith J, Bowman J, Cook-Deegan R, Cox D, Duster T, Eisenberg R, Fine B, Holtzman N, King P, Kitcher P, McInerney J, McKusick V, Mulvihill J, Murray J, Murray R, Murray T, Nelkin D, Rapp R, Saxton M, Wexler N. Allen A, et al. Am J Hum Genet. 1996 Aug;59(2):487-8. Am J Hum Genet. 1996. PMID: 8755944 Free PMC article. No abstract available.

8

Polymorphisms and rare sequence variants at the ROM1 locus.

Bascom RA, Liu L, Humphries P, Fishman GA, Murray JC, McInnes RR. Bascom RA, et al. Among authors: murray jc. Hum Mol Genet. 1993 Nov;2(11):1975-7. doi: 10.1093/hmg/2.11.1975. Hum Mol Genet. 1993. PMID: 7904211

9

Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site.

Siniscalco M, Oberlé I, Melis P, Alhadeff B, Murray J, Filippi G, Mattioni T, Chen YT, Furneaux H, Old LJ, et al. Siniscalco M, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):357-62. doi: 10.1002/ajmg.1320380239. Am J Med Genet. 1991. PMID: 1708201

10

Report of the committee on the genetic constitution of chromosome 4.

Cox D, Murray J. Cox D, et al. Cytogenet Cell Genet. 1988;49(1-3):52-4. doi: 10.1159/000132649. Cytogenet Cell Genet. 1988. PMID: 3203550 No abstract available.

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