Leversha M - Search Results

1

Cloning of the X-linked glycerol kinase deficiency gene and its identification by sequence comparison to the Bacillus subtilis homologue.

Sargent CA, Affara NA, Bentley E, Pelmear A, Bailey DM, Davey P, Dow D, Leversha M, Aplin H, Besley GT, et al. Sargent CA, et al. Among authors: leversha m. Hum Mol Genet. 1993 Feb;2(2):97-106. doi: 10.1093/hmg/2.2.97. Hum Mol Genet. 1993. PMID: 8499912

2

A rearrangement on chromosome 5 of an expressed human beta-glucuronidase pseudogene.

Sargent CA, Chalmers IJ, Leversha M, Affara NA. Sargent CA, et al. Among authors: leversha m. Mamm Genome. 1994 Dec;5(12):791-6. doi: 10.1007/BF00292015. Mamm Genome. 1994. PMID: 7894161

3

Molecular genetic analysis of the 3p- syndrome.

Phipps ME, Latif F, Prowse A, Payne SJ, Dietz-Band J, Leversha M, Affara NA, Moore AT, Tolmie J, Schinzel A, et al. Phipps ME, et al. Among authors: leversha m. Hum Mol Genet. 1994 Jun;3(6):903-8. doi: 10.1093/hmg/3.6.903. Hum Mol Genet. 1994. PMID: 7951234 Free article. Clinical Trial.

4

Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3.

Brown GM, Leversha M, Hulten M, Ferguson-Smith MA, Affara NA, Furlong RA. Brown GM, et al. Among authors: leversha m. Am J Hum Genet. 1998 Jun;62(6):1484-92. doi: 10.1086/301863. Am J Hum Genet. 1998. PMID: 9585591 Free PMC article.

5

Coincidence painting: a rapid method for cloning region specific DNA sequences.

Bailey DM, Carter NP, de Vos D, Leversha MA, Perryman MT, Ferguson-Smith MA. Bailey DM, et al. Among authors: leversha ma. Nucleic Acids Res. 1993 Nov 11;21(22):5117-23. doi: 10.1093/nar/21.22.5117. Nucleic Acids Res. 1993. PMID: 8255765 Free PMC article.

6

Structure and expression analysis of a member of the human glutamate dehydrogenase (GLUD) gene family mapped to chromosome 10p11.2.

Tzimagiorgis G, Leversha MA, Chroniary K, Goulielmos G, Sargent CA, Ferguson-Smith M, Moschonas NK. Tzimagiorgis G, et al. Among authors: leversha ma. Hum Genet. 1993 Jun;91(5):433-8. doi: 10.1007/BF00217767. Hum Genet. 1993. PMID: 8314555

7

Physical mapping of chromosome 3p25-p26 by fluorescence in situ hybridisation (FISH).

Phipps ME, Maher ER, Affara NA, Latif F, Leversha MA, Ferguson-Smith ME, Nakamura Y, Lerman M, Zbar B, Ferguson-Smith MA. Phipps ME, et al. Among authors: leversha ma. Hum Genet. 1993 Aug;92(1):18-22. doi: 10.1007/BF00216139. Hum Genet. 1993. PMID: 8365722

8

Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry.

Goudie DR, Yuille MA, Leversha MA, Furlong RA, Carter NP, Lush MJ, Affara NA, Ferguson-Smith MA. Goudie DR, et al. Among authors: leversha ma. Nat Genet. 1993 Feb;3(2):165-9. doi: 10.1038/ng0293-165. Nat Genet. 1993. PMID: 8499949

9

Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.

Carter NP, Ferguson-Smith MA, Perryman MT, Telenius H, Pelmear AH, Leversha MA, Glancy MT, Wood SL, Cook K, Dyson HM, et al. Carter NP, et al. Among authors: leversha ma. J Med Genet. 1992 May;29(5):299-307. doi: 10.1136/jmg.29.5.299. J Med Genet. 1992. PMID: 1583656 Free PMC article.

10

Physical analysis of the tuberous sclerosis region in 9q34.

Zhou CY, Wu KY, Leversha MA, Furlong RA, Ferguson-Smith MA, Affara NA. Zhou CY, et al. Among authors: leversha ma. Genomics. 1995 Jan 1;25(1):304-8. doi: 10.1016/0888-7543(95)80143-a. Genomics. 1995. PMID: 7774937

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