Mitchell M - Search Results

1

Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes.

Affara NA, Ferguson-Smith MA, Magenis RE, Tolmie JL, Boyd E, Cooke A, Jamieson D, Kwok K, Mitchell M, Snadden L. Affara NA, et al. Among authors: mitchell m. Nucleic Acids Res. 1987 Sep 25;15(18):7325-42. doi: 10.1093/nar/15.18.7325. Nucleic Acids Res. 1987. PMID: 3658694 Free PMC article.

2

Regional assignment of Y-linked DNA probes by deletion mapping and their homology with X-chromosome and autosomal sequences.

Affara NA, Florentin L, Morrison N, Kwok K, Mitchell M, Cook A, Jamieson D, Glasgow L, Meredith L, Boyd E, et al. Affara NA, et al. Among authors: mitchell m. Nucleic Acids Res. 1986 Jul 11;14(13):5353-73. doi: 10.1093/nar/14.13.5353. Nucleic Acids Res. 1986. PMID: 3737403 Free PMC article.

3

Variable transfer of Y-specific sequences in XX males.

Affara NA, Ferguson-Smith MA, Tolmie J, Kwok K, Mitchell M, Jamieson D, Cooke A, Florentin L. Affara NA, et al. Among authors: mitchell m. Nucleic Acids Res. 1986 Jul 11;14(13):5375-87. doi: 10.1093/nar/14.13.5375. Nucleic Acids Res. 1986. PMID: 3737404 Free PMC article.

4

The role of human and mouse Y chromosome genes in male infertility.

Affara NA, Mitchell MJ. Affara NA, et al. Among authors: mitchell mj. J Endocrinol Invest. 2000 Nov;23(10):630-45. doi: 10.1007/BF03343787. J Endocrinol Invest. 2000. PMID: 11097427 Review.

5

X chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis).

Cooke A, Gillard EF, Yates JR, Mitchell MJ, Aitken DA, Weir DM, Affara NA, Ferguson-Smith MA. Cooke A, et al. Among authors: mitchell mj. Hum Genet. 1988 May;79(1):49-52. doi: 10.1007/BF00291709. Hum Genet. 1988. PMID: 3163320

6

Analysis of sex chromosome abnormalities using X and Y chromosome DNA tiling path arrays.

Karcanias AC, Ichimura K, Mitchell MJ, Sargent CA, Affara NA. Karcanias AC, et al. Among authors: mitchell mj. J Med Genet. 2007 Jul;44(7):429-36. doi: 10.1136/jmg.2006.047852. Epub 2007 Feb 27. J Med Genet. 2007. PMID: 17327287 Free PMC article.

7

Physical mapping of deletion breakpoints in patients with X-linked ichthyosis: evidence for clustering of distal and proximal breakpoints.

Newman RS, Affara NA, Yates JR, Mitchell M, Ferguson-Smith MA. Newman RS, et al. Among authors: mitchell m. Proc Biol Sci. 1990 Dec 22;242(1305):231-9. doi: 10.1098/rspb.1990.0129. Proc Biol Sci. 1990. PMID: 1983039

8

Localization of murine X and autosomal sequences homologous to the human Y located testis-determining region.

Mitchell M, Simon D, Affara N, Ferguson-Smith M, Avner P, Bishop C. Mitchell M, et al. Genetics. 1989 Apr;121(4):803-9. doi: 10.1093/genetics/121.4.803. Genetics. 1989. PMID: 2721933 Free PMC article.

9

Report of the Second International Workshop on Y Chromosome Mapping 1995.

Affara N, Bishop C, Brown W, Cooke H, Davey P, Ellis N, Graves JM, Jones M, Mitchell M, Rappold G, Tyler-Smith C, Yen P, Lau YF. Affara N, et al. Among authors: mitchell m. Cytogenet Cell Genet. 1996;73(1-2):33-76. doi: 10.1159/000134310. Cytogenet Cell Genet. 1996. PMID: 8646888 No abstract available.

10

Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry gene.

Brown GM, Furlong RA, Sargent CA, Erickson RP, Longepied G, Mitchell M, Jones MH, Hargreave TB, Cooke HJ, Affara NA. Brown GM, et al. Among authors: mitchell m. Hum Mol Genet. 1998 Jan;7(1):97-107. doi: 10.1093/hmg/7.1.97. Hum Mol Genet. 1998. PMID: 9384609

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