Murray JC - Search Results

1

Characterization of the human HOX 7 cDNA and identification of polymorphic markers.

Padanilam BJ, Stadler HS, Mills KA, McLeod LB, Solursh M, Lee B, Ramirez F, Buetow KH, Murray JC. Padanilam BJ, et al. Among authors: murray jc. Hum Mol Genet. 1992 Sep;1(6):407-10. doi: 10.1093/hmg/1.6.407. Hum Mol Genet. 1992. PMID: 1284527

2

Tetranucleotide repeat polymorphism at the human alpha fibrinogen locus (FGA).

Mills KA, Even D, Murray JC. Mills KA, et al. Among authors: murray jc. Hum Mol Genet. 1992 Dec;1(9):779. doi: 10.1093/hmg/1.9.779. Hum Mol Genet. 1992. PMID: 1302622 No abstract available.

3

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

4

Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4.

Stadler HS, Padanilam BJ, Buetow K, Murray JC, Solursh M. Stadler HS, et al. Among authors: murray jc. Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11579-83. doi: 10.1073/pnas.89.23.11579. Proc Natl Acad Sci U S A. 1992. PMID: 1360670 Free PMC article.

5

Genetic and physical maps of human chromosome 4 based on dinucleotide repeats.

Mills KA, Buetow KH, Xu Y, Weber JL, Altherr MR, Wasmuth JJ, Murray JC. Mills KA, et al. Among authors: murray jc. Genomics. 1992 Oct;14(2):209-19. doi: 10.1016/s0888-7543(05)80208-3. Genomics. 1992. PMID: 1427835

6

Genetic marker study of dentinogenesis imperfecta.

Crall MG, Schuler CF, Buetow KH, Murray JC. Crall MG, et al. Among authors: murray jc. Proc Finn Dent Soc. 1992;88 Suppl 1:285-93. Proc Finn Dent Soc. 1992. PMID: 1508884

7

Construction of a human chromosome 4 YAC pool and analysis of artificial chromosome stability.

Sleister HM, Mills KA, Blackwell SE, Killary AM, Murray JC, Malone RE. Sleister HM, et al. Among authors: murray jc. Nucleic Acids Res. 1992 Jul 11;20(13):3419-25. doi: 10.1093/nar/20.13.3419. Nucleic Acids Res. 1992. PMID: 1630913 Free PMC article.

8

Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.

Mathews KD, Mills KA, Bosch EP, Ionasescu VV, Wiles KR, Buetow KH, Murray JC. Mathews KD, et al. Among authors: murray jc. Am J Hum Genet. 1992 Aug;51(2):428-31. Am J Hum Genet. 1992. PMID: 1642242 Free PMC article.

9

Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).

Mills KA, Buetow KH, Xu Y, Ritty TM, Mathews KD, Bodrug SE, Wijmenga C, Balazs I, Murray JC. Mills KA, et al. Among authors: murray jc. Am J Hum Genet. 1992 Aug;51(2):432-9. Am J Hum Genet. 1992. PMID: 1642243 Free PMC article.

10

A detailed multipoint gene map of chromosome 1q.

Buetow KH, Nishimura D, Nakamura Y, Jiang O, Murray JC. Buetow KH, et al. Among authors: murray jc. Genomics. 1990 Sep;8(1):13-21. doi: 10.1016/0888-7543(90)90220-o. Genomics. 1990. PMID: 1981991

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