Boyd Y - Search Results

1

The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysis.

Robinson DO, Boyd Y, Cockburn D, Collinson MN, Craig I, Jacobs PA. Robinson DO, et al. Among authors: boyd y. Genet Res. 1990 Oct-Dec;56(2-3):135-40. doi: 10.1017/s0016672300035217. Genet Res. 1990. PMID: 2272503

2

Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy.

Boyd Y, Cockburn D, Holt S, Munro E, Van Ommen GJ, Gillard B, Affara N, Ferguson-Smith M, Craig I. Boyd Y, et al. Cytogenet Cell Genet. 1988;48(1):28-34. doi: 10.1159/000132581. Cytogenet Cell Genet. 1988. PMID: 3180845

3

Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresis.

Meitinger T, Boyd Y, Anand R, Craig IW. Meitinger T, et al. Among authors: boyd y. Genomics. 1988 Nov;3(4):315-22. doi: 10.1016/0888-7543(88)90122-x. Genomics. 1988. PMID: 3243546

4

Molecular heterogeneity of translocations associated with muscular dystrophy.

Boyd Y, Munro E, Ray P, Worton R, Monaco T, Kunkel L, Craig I. Boyd Y, et al. Clin Genet. 1987 Apr;31(4):265-72. doi: 10.1111/j.1399-0004.1987.tb02805.x. Clin Genet. 1987. PMID: 3594934

5

Muscular dystrophy in girls with X;autosome translocations.

Boyd Y, Buckle V, Holt S, Munro E, Hunter D, Craig I. Boyd Y, et al. J Med Genet. 1986 Dec;23(6):484-90. doi: 10.1136/jmg.23.6.484. J Med Genet. 1986. PMID: 3806636 Free PMC article.

6

Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophy.

van Bakel I, Holt S, Craig I, Boyd Y. van Bakel I, et al. Among authors: boyd y. Am J Hum Genet. 1995 Aug;57(2):329-36. Am J Hum Genet. 1995. PMID: 7668258 Free PMC article.

7

Mapping of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin gene.

Cockburn DJ, Munro EA, Craig IW, Boyd Y. Cockburn DJ, et al. Among authors: boyd y. Hum Genet. 1992 Dec;90(4):407-12. doi: 10.1007/BF00220468. Hum Genet. 1992. PMID: 1483697

8

Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22.

Fraser NJ, Boyd Y, Craig I. Fraser NJ, et al. Among authors: boyd y. Genomics. 1989 Jul;5(1):144-8. doi: 10.1016/0888-7543(89)90099-2. Genomics. 1989. PMID: 2570025

9

Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q.

Schonk D, Coerwinkel-Driessen M, van Dalen I, Oerlemans F, Smeets B, Schepens J, Hulsebos T, Cockburn D, Boyd Y, Davis M, et al. Schonk D, et al. Among authors: boyd y. Genomics. 1989 Apr;4(3):384-96. doi: 10.1016/0888-7543(89)90346-7. Genomics. 1989. PMID: 2714797

10

Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].

Fraser NJ, Boyd Y, Brownlee GG, Craig IW. Fraser NJ, et al. Among authors: boyd y. Nucleic Acids Res. 1987 Nov 25;15(22):9616. doi: 10.1093/nar/15.22.9616. Nucleic Acids Res. 1987. PMID: 2891116 Free PMC article. No abstract available.

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