Boyle S - Search Results

1

Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: a possible contributor to the holoprosencephaly 3 phenotype.

Mackay M, Fantes J, Scherer S, Boyle S, West K, Tsui LC, Belloni E, Lutz E, Van Heyningen V, Harmar AJ. Mackay M, et al. Among authors: boyle s. Genomics. 1996 Nov 1;37(3):345-53. doi: 10.1006/geno.1996.0569. Genomics. 1996. PMID: 8938447

2

Direct microdissection and microcloning of a translocation breakpoint region, t(1;11)(q42.2;q21), associated with schizophrenia.

Muir WJ, Gosden CM, Brookes AJ, Fantes J, Evans KL, Maguire SM, Stevenson B, Boyle S, Blackwood DH, St Clair DM, et al. Muir WJ, et al. Among authors: boyle s. Cytogenet Cell Genet. 1995;70(1-2):35-40. doi: 10.1159/000133986. Cytogenet Cell Genet. 1995. PMID: 7736785

3

A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: distal p13 to proximal p15.1.

Fantes JA, Oghene K, Boyle S, Danes S, Fletcher JM, Bruford EA, Williamson K, Seawright A, Schedl A, Hanson I, et al. Fantes JA, et al. Among authors: boyle s. Genomics. 1995 Jan 20;25(2):447-61. doi: 10.1016/0888-7543(95)80045-n. Genomics. 1995. PMID: 7789978

4

Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype.

Fantes J, Redeker B, Breen M, Boyle S, Brown J, Fletcher J, Jones S, Bickmore W, Fukushima Y, Mannens M, et al. Fantes J, et al. Among authors: boyle s. Hum Mol Genet. 1995 Mar;4(3):415-22. doi: 10.1093/hmg/4.3.415. Hum Mol Genet. 1995. PMID: 7795596

5

Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3.

Brown J, Dry KL, Edgar AJ, Pryde FE, Hardwick LJ, Aldred MA, Lester DH, Boyle S, Kaplan J, Dufier JL, Ho MF, Monaco AM, Musarella MA, Wright AF. Brown J, et al. Among authors: boyle s. Genomics. 1996 Oct 15;37(2):200-10. doi: 10.1006/geno.1996.0543. Genomics. 1996. PMID: 8921393

6

The reticulocalbin gene maps to the WAGR region in human and to the Small eye Harwell deletion in mouse.

Kent J, Lee M, Schedl A, Boyle S, Fantes J, Powell M, Rushmere N, Abbott C, van Heyningen V, Bickmore WA. Kent J, et al. Among authors: boyle s. Genomics. 1997 Jun 1;42(2):260-7. doi: 10.1006/geno.1997.4706. Genomics. 1997. PMID: 9192846

7

Molecular cloning of a human cDNA IGSF3 encoding an immunoglobulin-like membrane protein: expression and mapping to chromosome band 1p13.

Saupe S, Roizès G, Peter M, Boyle S, Gardiner K, De Sario A. Saupe S, et al. Among authors: boyle s. Genomics. 1998 Sep 15;52(3):305-11. doi: 10.1006/geno.1998.5439. Genomics. 1998. PMID: 9790749

8

Human (DACH) and mouse (Dach) homologues of Drosophila dachshund map to chromosomes 13q22 and 14E3, respectively.

Hammond KL, Lettice LA, Hill RE, Lee M, Boyle S, Hanson IM. Hammond KL, et al. Among authors: boyle s. Genomics. 1999 Jan 15;55(2):252-3. doi: 10.1006/geno.1998.5662. Genomics. 1999. PMID: 9933575 No abstract available.

9

Differences in the localization and morphology of chromosomes in the human nucleus.

Croft JA, Bridger JM, Boyle S, Perry P, Teague P, Bickmore WA. Croft JA, et al. Among authors: boyle s. J Cell Biol. 1999 Jun 14;145(6):1119-31. doi: 10.1083/jcb.145.6.1119. J Cell Biol. 1999. PMID: 10366586 Free PMC article.

10

Condensation behaviour of the human X chromosome in male germ cells and Sertoli cells examined by fluorescence in situ hybridization.

Kofman-Alfaro S, Speed RM, Boyle S, Chandley AC. Kofman-Alfaro S, et al. Among authors: boyle s. Chromosome Res. 1994 Nov;2(6):439-44. doi: 10.1007/BF01552866. Chromosome Res. 1994. PMID: 7834220

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