Joyce JA - Search Results

1

A frequent hMSH2 mutation in hereditary non-polyposis colon cancer syndrome.

Froggatt NJ, Joyce JA, Davies R, Gareth D, Evans R, Ponder BA, Barton DE, Maher ER. Froggatt NJ, et al. Among authors: joyce ja. Lancet. 1995 Mar 18;345(8951):727. doi: 10.1016/s0140-6736(95)90900-1. Lancet. 1995. PMID: 7885145 No abstract available.

2

Molecular genetic analysis of exons 1 to 6 of the APC gene in non-polyposis familial colorectal cancer.

Joyce JA, Froggatt NJ, Davies R, Evans DG, Trembath R, Barton DE, Maher ER. Joyce JA, et al. Clin Genet. 1995 Dec;48(6):299-303. doi: 10.1111/j.1399-0004.1995.tb04113.x. Clin Genet. 1995. PMID: 8835324

3

MSH2 sequence variations and inherited colorectal cancer susceptibility.

Froggatt NJ, Joyce JA, Evans DG, Lunt PW, Koch DJ, Ponder BJ, Maher ER. Froggatt NJ, et al. Among authors: joyce ja. Eur J Cancer. 1996 Jan;32A(1):178. doi: 10.1016/0959-8049(95)00464-5. Eur J Cancer. 1996. PMID: 8695231 No abstract available.

4

Microsatellite instability in early onset and familial colorectal cancer.

Brassett C, Joyce JA, Froggatt NJ, Williams G, Furniss D, Walsh S, Miller R, Evans DG, Maher ER. Brassett C, et al. Among authors: joyce ja. J Med Genet. 1996 Dec;33(12):981-5. doi: 10.1136/jmg.33.12.981. J Med Genet. 1996. PMID: 9004127 Free PMC article.

5

Genomic imprinting and cancer; new paradigms in the genetics of neoplasia.

Schofield PN, Joyce JA, Lam WK, Grandjean V, Ferguson-Smith A, Reik W, Maher ER. Schofield PN, et al. Among authors: joyce ja. Toxicol Lett. 2001 Mar 31;120(1-3):151-60. doi: 10.1016/s0378-4274(01)00294-6. Toxicol Lett. 2001. PMID: 11323172 Review.

6

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.

Catchpoole D, Lam WW, Valler D, Temple IK, Joyce JA, Reik W, Schofield PN, Maher ER. Catchpoole D, et al. Among authors: joyce ja. J Med Genet. 1997 May;34(5):353-9. doi: 10.1136/jmg.34.5.353. J Med Genet. 1997. PMID: 9152830 Free PMC article.

7

Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome.

Joyce JA, Lam WK, Catchpoole DJ, Jenks P, Reik W, Maher ER, Schofield PN. Joyce JA, et al. Hum Mol Genet. 1997 Sep;6(9):1543-8. doi: 10.1093/hmg/6.9.1543. Hum Mol Genet. 1997. PMID: 9285792

8

Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome.

Catchpoole D, Smallwood AV, Joyce JA, Murrell A, Lam W, Tang T, Munroe D, Reik W, Schofield PN, Maher ER. Catchpoole D, et al. Among authors: joyce ja. J Med Genet. 2000 Mar;37(3):212-5. doi: 10.1136/jmg.37.3.212. J Med Genet. 2000. PMID: 10777363 Free PMC article. No abstract available.

9

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome.

Smilinich NJ, Day CD, Fitzpatrick GV, Caldwell GM, Lossie AC, Cooper PR, Smallwood AC, Joyce JA, Schofield PN, Reik W, Nicholls RD, Weksberg R, Driscoll DJ, Maher ER, Shows TB, Higgins MJ. Smilinich NJ, et al. Among authors: joyce ja. Proc Natl Acad Sci U S A. 1999 Jul 6;96(14):8064-9. doi: 10.1073/pnas.96.14.8064. Proc Natl Acad Sci U S A. 1999. PMID: 10393948 Free PMC article.

10

Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation.

Lam WW, Hatada I, Ohishi S, Mukai T, Joyce JA, Cole TR, Donnai D, Reik W, Schofield PN, Maher ER. Lam WW, et al. Among authors: joyce ja. J Med Genet. 1999 Jul;36(7):518-23. J Med Genet. 1999. PMID: 10424811 Free PMC article.

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