Smith MJ - Search Results

1

The genomic organisation of the human pseudoautosomal gene MIC2 and the detection of a related locus.

Smith MJ, Goodfellow PJ, Goodfellow PN. Smith MJ, et al. Hum Mol Genet. 1993 Apr;2(4):417-22. doi: 10.1093/hmg/2.4.417. Hum Mol Genet. 1993. PMID: 8504302

2

MIC2R: a transcribed MIC2-related sequence associated with a CpG island in the human pseudoautosomal region.

Smith MJ, Goodfellow PN. Smith MJ, et al. Hum Mol Genet. 1994 Sep;3(9):1575-82. doi: 10.1093/hmg/3.9.1575. Hum Mol Genet. 1994. PMID: 7833914

3

MIC2: a human pseudoautosomal gene.

Goodfellow PN, Pym B, Pritchard C, Ellis N, Palmer M, Smith M, Goodfellow PJ. Goodfellow PN, et al. Philos Trans R Soc Lond B Biol Sci. 1988 Dec 1;322(1208):145-54. doi: 10.1098/rstb.1988.0122. Philos Trans R Soc Lond B Biol Sci. 1988. PMID: 2907798

4

The pseudoautosomal boundary in man is defined by an Alu repeat sequence inserted on the Y chromosome.

Ellis NA, Goodfellow PJ, Pym B, Smith M, Palmer M, Frischauf AM, Goodfellow PN. Ellis NA, et al. Nature. 1989 Jan 5;337(6202):81-4. doi: 10.1038/337081a0. Nature. 1989. PMID: 2909893

5

Gene mapping and genetic diseases.

Smith MJ, Goodfellow PN. Smith MJ, et al. Curr Opin Cell Biol. 1989 Jun;1(3):460-5. doi: 10.1016/0955-0674(89)90006-9. Curr Opin Cell Biol. 1989. PMID: 2534043 Review. No abstract available.

6

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif.

Sinclair AH, Berta P, Palmer MS, Hawkins JR, Griffiths BL, Smith MJ, Foster JW, Frischauf AM, Lovell-Badge R, Goodfellow PN. Sinclair AH, et al. Among authors: smith mj. Nature. 1990 Jul 19;346(6281):240-4. doi: 10.1038/346240a0. Nature. 1990. PMID: 1695712

7

SOX14 is a candidate gene for limb defects associated with BPES and Möbius syndrome.

Wilmore HP, Smith MJ, Wilcox SA, Bell KM, Sinclair AH. Wilmore HP, et al. Among authors: smith mj. Hum Genet. 2000 Mar;106(3):269-76. doi: 10.1007/s004390051037. Hum Genet. 2000. PMID: 10798354

8

Familial Kallmann syndrome: a novel splice acceptor mutation in the KAL gene.

O'Neill MJ, Tridjaja B, Smith MJ, Bell KM, Warne GL, Sinclair AH. O'Neill MJ, et al. Among authors: smith mj. Hum Mutat. 1998;11(4):340-2. Hum Mutat. 1998. PMID: 9554756

9

Sex determination. Turning on sex.

Smith MJ. Smith MJ. Curr Biol. 1994 Nov 1;4(11):1003-5. doi: 10.1016/s0960-9822(00)00226-8. Curr Biol. 1994. PMID: 7874479 Review.

10

Novel mutation in the SRY gene results in 46,XY gonadal dysgenesis.

Cameron FJ, Smith MJ, Warne GL, Sinclair AH. Cameron FJ, et al. Among authors: smith mj. Hum Mutat. 1998;Suppl 1:S110-1. doi: 10.1002/humu.1380110136. Hum Mutat. 1998. PMID: 9452057 No abstract available.

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