Scambler P - Search Results

1

Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3).

Dechairo B, Dimon C, van Heel D, Mackay I, Edwards M, Scambler P, Jewell D, Cardon L, Lench N, Carey A. Dechairo B, et al. Among authors: scambler p. Eur J Hum Genet. 2001 Aug;9(8):627-33. doi: 10.1038/sj.ejhg.5200687. Eur J Hum Genet. 2001. PMID: 11528509

2

RFLP for C2/11 (D7S374), a cosmid for chromosome seven.

Scambler PJ, Lench NJ. Scambler PJ, et al. Nucleic Acids Res. 1987 Oct 12;15(19):8121. doi: 10.1093/nar/15.19.8121. Nucleic Acids Res. 1987. PMID: 2890139 Free PMC article.

3

A human regulatory subunit of type II cAMP-dependent protein kinase localized by its linkage relationship to several cloned chromosome 7q markers.

Wainwright B, Lench N, Davies K, Scambler P, Kruyer H, Williamson R, Jahnsen T, Farrall M. Wainwright B, et al. Among authors: scambler p. Cytogenet Cell Genet. 1987;45(3-4):237-9. doi: 10.1159/000132461. Cytogenet Cell Genet. 1987. PMID: 3691190 No abstract available.

4

Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.

Halford S, Lindsay E, Nayudu M, Carey AH, Baldini A, Scambler PJ. Halford S, et al. Among authors: scambler pj. Hum Mol Genet. 1993 Feb;2(2):191-6. doi: 10.1093/hmg/2.2.191. Hum Mol Genet. 1993. PMID: 8499906

5

An anonymous DNA probe (NL32) recognises a MspI polymorphism on human chromosome 1 [D1S84].

Lench NJ, Scambler PJ. Lench NJ, et al. Among authors: scambler pj. Nucleic Acids Res. 1988 Dec 23;16(24):11854. doi: 10.1093/nar/16.24.11854. Nucleic Acids Res. 1988. PMID: 2463518 Free PMC article.

6

Interstitial deletions in DiGeorge syndrome detected with microclones from 22q11.

Carey AH, Claussen U, Lüdecke HJ, Horsthemke B, Ellis D, Oakey H, Wilson D, Burn J, Williamson R, Scambler PJ. Carey AH, et al. Among authors: scambler pj. Mamm Genome. 1992;3(2):101-5. doi: 10.1007/BF00431253. Mamm Genome. 1992. PMID: 1617213

7

Cystic fibrosis linkage exclusion data.

Scambler PJ, Bell G, Watson E, Farrall M, Bates G, Davies K, Lench N, Ashworth A, Williamson R, Tippett P, et al. Scambler PJ, et al. Cytogenet Cell Genet. 1986;41(1):62-3. doi: 10.1159/000132200. Cytogenet Cell Genet. 1986. PMID: 3455913 No abstract available.

8

Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.

Kelly D, Goldberg R, Wilson D, Lindsay E, Carey A, Goodship J, Burn J, Cross I, Shprintzen RJ, Scambler PJ. Kelly D, et al. Among authors: scambler pj. Am J Med Genet. 1993 Feb 1;45(3):308-12. doi: 10.1002/ajmg.1320450306. Am J Med Genet. 1993. PMID: 8434616

9

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

Scambler PJ, Carey AH, Wyse RK, Roach S, Dumanski JP, Nordenskjold M, Williamson R. Scambler PJ, et al. Genomics. 1991 May;10(1):201-6. doi: 10.1016/0888-7543(91)90501-5. Genomics. 1991. PMID: 2045103

10

Linkage of COL1A2 collagen gene to cystic fibrosis, and its clinical implications.

Scambler PJ, Wainwright BJ, Farrall M, Bell J, Stanier P, Lench NJ, Bell G, Kruyer H, Ramirez F, Williamson R. Scambler PJ, et al. Lancet. 1985 Nov 30;2(8466):1241-2. doi: 10.1016/s0140-6736(85)90765-2. Lancet. 1985. PMID: 2866313 No abstract available.

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