Fox M - Search Results

1

Genetic and physical mapping of the CLN6 gene on chromosome 15q21-23.

Sharp JD, Wheeler RB, Lake BD, Fox M, Gardiner RM, Williams RE. Sharp JD, et al. Among authors: fox m. Mol Genet Metab. 1999 Apr;66(4):329-31. doi: 10.1006/mgme.1999.2806. Mol Genet Metab. 1999. PMID: 10191123

2

Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD).

Kermani S, Gregory-Evans K, Tarttelin EE, Bellingham J, Plant C, Bird AC, Fox M, Bhattacharya SS, Gregory-Evans CY. Kermani S, et al. Among authors: fox m. Hum Genet. 1999 Jan;104(1):77-82. doi: 10.1007/s004390050913. Hum Genet. 1999. PMID: 10071196

3

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.

Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP. Lai CS, et al. Among authors: fox m. Am J Hum Genet. 2000 Aug;67(2):357-68. doi: 10.1086/303011. Epub 2000 Jul 5. Am J Hum Genet. 2000. PMID: 10880297 Free PMC article.

4

Structure of the human N-cadherin gene: YAC analysis and fine chromosomal mapping to 18q11.2.

Wallis J, Fox MF, Walsh FS. Wallis J, et al. Among authors: fox mf. Genomics. 1994 Jul 1;22(1):172-9. doi: 10.1006/geno.1994.1358. Genomics. 1994. PMID: 7959764

5

Localization of genes encoding three distinct flavin-containing monooxygenases to human chromosome 1q.

Shephard EA, Dolphin CT, Fox MF, Povey S, Smith R, Phillips IR. Shephard EA, et al. Among authors: fox mf. Genomics. 1993 Apr;16(1):85-9. doi: 10.1006/geno.1993.1144. Genomics. 1993. PMID: 8486388

6

Irradiation hybrids for human chromosome 11: characterization and use for generating region-specific markers in 11q14-q23.

Gillett GT, McConville CM, Byrd PJ, Stankovic T, Taylor AM, Hunt DM, West LF, Fox MF, Povey S, Benham FJ. Gillett GT, et al. Among authors: fox mf. Genomics. 1993 Feb;15(2):332-41. doi: 10.1006/geno.1993.1065. Genomics. 1993. PMID: 8449499

7

The human TBX6 gene: cloning and assignment to chromosome 16p11.2.

Papapetrou C, Putt W, Fox M, Edwards YH. Papapetrou C, et al. Among authors: fox m. Genomics. 1999 Jan 15;55(2):238-41. doi: 10.1006/geno.1998.5646. Genomics. 1999. PMID: 9933572

8

Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma.

Lehmann OJ, Ebenezer ND, Jordan T, Fox M, Ocaka L, Payne A, Leroy BP, Clark BJ, Hitchings RA, Povey S, Khaw PT, Bhattacharya SS. Lehmann OJ, et al. Among authors: fox m. Am J Hum Genet. 2000 Nov;67(5):1129-35. doi: 10.1016/S0002-9297(07)62943-7. Epub 2000 Sep 27. Am J Hum Genet. 2000. PMID: 11007653 Free PMC article.

9

Regional localization of the intestinal mucin gene MUC3 to chromosome 7q22.

Fox MF, Lahbib F, Pratt W, Attwood J, Gum J, Kim Y, Swallow DM. Fox MF, et al. Ann Hum Genet. 1992 Oct;56(4):281-7. doi: 10.1111/j.1469-1809.1992.tb01154.x. Ann Hum Genet. 1992. PMID: 1362870

10

Regional localization of the lactase-phlorizin hydrolase gene, LCT, to chromosome 2q21.

Harvey CB, Fox MF, Jeggo PA, Mantei N, Povey S, Swallow DM. Harvey CB, et al. Among authors: fox mf. Ann Hum Genet. 1993 Jul;57(3):179-85. doi: 10.1111/j.1469-1809.1993.tb01593.x. Ann Hum Genet. 1993. PMID: 8257087

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