Walker AP - Search Results

1

Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombination.

Den Dunnen JT, Grootscholten PM, Dauwerse JG, Walker AP, Monaco AP, Butler R, Anand R, Coffey AJ, Bentley DR, Steensma HY, et al. Den Dunnen JT, et al. Among authors: walker ap. Hum Mol Genet. 1992 Apr;1(1):19-28. doi: 10.1093/hmg/1.1.19. Hum Mol Genet. 1992. PMID: 1301131

2

Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters.

Górecki DC, Monaco AP, Derry JM, Walker AP, Barnard EA, Barnard PJ. Górecki DC, et al. Among authors: walker ap. Hum Mol Genet. 1992 Oct;1(7):505-10. doi: 10.1093/hmg/1.7.505. Hum Mol Genet. 1992. PMID: 1307251

3

A yeast artificial chromosome contig containing the complete Duchenne muscular dystrophy gene.

Monaco AP, Walker AP, Millwood I, Larin Z, Lehrach H. Monaco AP, et al. Among authors: walker ap. Genomics. 1992 Mar;12(3):465-73. doi: 10.1016/0888-7543(92)90436-v. Genomics. 1992. PMID: 1559698

4

Isolation of the human Xp21 glycerol kinase gene by positional cloning.

Walker AP, Muscatelli F, Monaco AP. Walker AP, et al. Hum Mol Genet. 1993 Feb;2(2):107-14. doi: 10.1093/hmg/2.2.107. Hum Mol Genet. 1993. PMID: 8499898

5

Mutations and phenotype in isolated glycerol kinase deficiency.

Walker AP, Muscatelli F, Stafford AN, Chelly J, Dahl N, Blomquist HK, Delanghe J, Willems PJ, Steinmann B, Monaco AP. Walker AP, et al. Am J Hum Genet. 1996 Jun;58(6):1205-11. Am J Hum Genet. 1996. PMID: 8651297 Free PMC article.

6

Isolation and characterization of a MAGE gene family in the Xp21.3 region.

Muscatelli F, Walker AP, De Plaen E, Stafford AN, Monaco AP. Muscatelli F, et al. Among authors: walker ap. Proc Natl Acad Sci U S A. 1995 May 23;92(11):4987-91. doi: 10.1073/pnas.92.11.4987. Proc Natl Acad Sci U S A. 1995. PMID: 7761436 Free PMC article.

7

A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes.

Walker AP, Chelly J, Love DR, Brush YI, Récan D, Chaussain JL, Oley CA, Connor JM, Yates J, Price DA, et al. Walker AP, et al. Hum Mol Genet. 1992 Nov;1(8):579-85. doi: 10.1093/hmg/1.8.579. Hum Mol Genet. 1992. PMID: 1301166

8

Gene deletion causing adrenal hypoplasia congenita and hypogonadotrophic hypogonadism.

Matfin G, Sheaves R, Muscatelli F, Walker A, Monaco A, Grant D, Nwose O, Wass JA. Matfin G, et al. Clin Endocrinol (Oxf). 1994 Jun;40(6):807-8. doi: 10.1111/j.1365-2265.1994.tb02517.x. Clin Endocrinol (Oxf). 1994. PMID: 8033374

9

Analysis of the primary sex ratio, sex chromosome aneuploidy and diploidy in human sperm using dual-colour fluorescence in situ hybridisation.

Goldman AS, Fomina Z, Knights PA, Hill CJ, Walker AP, Hultén MA. Goldman AS, et al. Among authors: walker ap. Eur J Hum Genet. 1993;1(4):325-34. doi: 10.1159/000472431. Eur J Hum Genet. 1993. PMID: 8081946

10

Two dinucleotide repeat polymorphisms at the DMD locus.

King SC, Stapleton PM, Walker AP, Love DR. King SC, et al. Among authors: walker ap. Hum Mol Genet. 1994 Mar;3(3):523. doi: 10.1093/hmg/3.3.523. Hum Mol Genet. 1994. PMID: 8012374 No abstract available.

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