Moore G - Search Results

1

Construction of a genetic map of human chromosome 17 by use of chromosome-mediated gene transfer.

Xu WM, Gorman PA, Rider SH, Hedge PJ, Moore G, Prichard C, Sheer D, Solomon E. Xu WM, et al. Among authors: moore g. Proc Natl Acad Sci U S A. 1988 Nov;85(22):8563-7. doi: 10.1073/pnas.85.22.8563. Proc Natl Acad Sci U S A. 1988. PMID: 3186746 Free PMC article.

2

Multiple tandem 18-kb sequences clustered in the region of the acute promyelocytic leukemia breakpoint on chromosome 17.

Moore G, Hedge PJ, Rider SH, Xu W, Hing S, Palmer R, Sheer D, Solomon E. Moore G, et al. Genomics. 1989 Feb;4(2):152-61. doi: 10.1016/0888-7543(89)90294-2. Genomics. 1989. PMID: 2737676

3

Localization of the oncogene c-erbA2 to human chromosome 3.

Rider SH, Gorman PA, Shipley JM, Moore G, Vennstrom B, Solomon E, Sheer D. Rider SH, et al. Among authors: moore g. Ann Hum Genet. 1987 May;51(2):153-60. doi: 10.1111/j.1469-1809.1987.tb01057.x. Ann Hum Genet. 1987. PMID: 3674756

4

Progress towards construction of a total restriction fragment map of a human chromosome.

Vissing H, Grosveld F, Solomon E, Moore G, Lench N, Shennan N, Williamson R. Vissing H, et al. Among authors: moore g. Nucleic Acids Res. 1987 Feb 25;15(4):1363-75. doi: 10.1093/nar/15.4.1363. Nucleic Acids Res. 1987. PMID: 3029713 Free PMC article.

5

Genetic basis of neural tube defects: the mouse gene loop-tail maps to a region of chromosome 1 syntenic with human 1q21-q23.

Stanier P, Henson JN, Eddleston J, Moore GE, Copp AJ. Stanier P, et al. Among authors: moore ge. Genomics. 1995 Apr 10;26(3):473-8. doi: 10.1016/0888-7543(95)80165-i. Genomics. 1995. PMID: 7607670

6

Limited evolutionary conservation of imprinting in the human placenta.

Monk D, Arnaud P, Apostolidou S, Hills FA, Kelsey G, Stanier P, Feil R, Moore GE. Monk D, et al. Among authors: moore ge. Proc Natl Acad Sci U S A. 2006 Apr 25;103(17):6623-8. doi: 10.1073/pnas.0511031103. Epub 2006 Apr 13. Proc Natl Acad Sci U S A. 2006. PMID: 16614068 Free PMC article.

7

Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.

Forbes SA, Brennan L, Richardson M, Coffey A, Cole CG, Gregory SG, Bentley DR, Mumm S, Moore GE, Stanier P. Forbes SA, et al. Among authors: moore ge. Genomics. 1996 Jan 1;31(1):36-43. doi: 10.1006/geno.1996.0006. Genomics. 1996. PMID: 8808277

8

Molecular approaches to dysmorphology.

Ivens A, Moore G, Williamson R. Ivens A, et al. Among authors: moore g. J Med Genet. 1988 Jul;25(7):473-9. doi: 10.1136/jmg.25.7.473. J Med Genet. 1988. PMID: 2902228 Free PMC article. Review.

9

X chromosome genes involved in the regulation of facial clefting and spina bifida.

Moore GE, Ivens A, Newton R, Balacs MA, Henderson DJ, Jensson O. Moore GE, et al. Cleft Palate J. 1990 Apr;27(2):131-5. doi: 10.1597/1545-1569(1990)027<0131:xcgiit>2.3.co;2. Cleft Palate J. 1990. PMID: 2187632 Review.

10

An analysis of common isodisomic regions in five mUPD 16 probands.

Abu-Amero SN, Ali Z, Abu-Amero KK, Stanier P, Moore GE. Abu-Amero SN, et al. Among authors: moore ge. J Med Genet. 1999 Mar;36(3):204-7. J Med Genet. 1999. PMID: 10204845 Free PMC article.

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