Maher ER - Search Results

1

Familial gastric cancer: overview and guidelines for management.

Caldas C, Carneiro F, Lynch HT, Yokota J, Wiesner GL, Powell SM, Lewis FR, Huntsman DG, Pharoah PD, Jankowski JA, MacLeod P, Vogelsang H, Keller G, Park KG, Richards FM, Maher ER, Gayther SA, Oliveira C, Grehan N, Wight D, Seruca R, Roviello F, Ponder BA, Jackson CE. Caldas C, et al. Among authors: maher er. J Med Genet. 1999 Dec;36(12):873-80. J Med Genet. 1999. PMID: 10593993 Free PMC article. Review.

2

Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markers.

Maher ER, Bentley E, Payne SJ, Latif F, Richards FM, Chiano M, Hosoe S, Yates JR, Linehan M, Barton DE, et al. Maher ER, et al. J Med Genet. 1992 Dec;29(12):902-5. doi: 10.1136/jmg.29.12.902. J Med Genet. 1992. PMID: 1362224 Free PMC article.

3

Three cases of 16q duplication.

Maher ER, Willatt L, Cuthbert G, Chapman C, Hodgson SV. Maher ER, et al. J Med Genet. 1991 Nov;28(11):801-2. doi: 10.1136/jmg.28.11.801. J Med Genet. 1991. PMID: 1820771 Free PMC article. No abstract available.

4

Von Hippel-Lindau disease: a genetic study.

Maher ER, Iselius L, Yates JR, Littler M, Benjamin C, Harris R, Sampson J, Williams A, Ferguson-Smith MA, Morton N. Maher ER, et al. J Med Genet. 1991 Jul;28(7):443-7. doi: 10.1136/jmg.28.7.443. J Med Genet. 1991. PMID: 1895313 Free PMC article.

5

Mapping of von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis.

Maher ER, Bentley E, Yates JR, Barton D, Jennings A, Fellows IW, Ponder MA, Ponder BA, Benjamin C, Harris R, et al. Maher ER, et al. J Neurol Sci. 1990 Dec;100(1-2):27-30. doi: 10.1016/0022-510x(90)90008-b. J Neurol Sci. 1990. PMID: 1982450

6

Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma.

Maher ER, Yates JR, Ferguson-Smith MA. Maher ER, et al. J Med Genet. 1990 May;27(5):311-4. doi: 10.1136/jmg.27.5.311. J Med Genet. 1990. PMID: 2352258 Free PMC article.

7

Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II.

Neumann HP, Eng C, Mulligan LM, Glavac D, Zäuner I, Ponder BA, Crossey PA, Maher ER, Brauch H. Neumann HP, et al. Among authors: maher er. JAMA. 1995 Oct 11;274(14):1149-51. JAMA. 1995. PMID: 7563486

8

Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.

Slatter RE, Elliott M, Welham K, Carrera M, Schofield PN, Barton DE, Maher ER. Slatter RE, et al. Among authors: maher er. J Med Genet. 1994 Oct;31(10):749-53. doi: 10.1136/jmg.31.10.749. J Med Genet. 1994. PMID: 7837249 Free PMC article.

9

TaqI and PstI RFLPs in the von Hippel-Lindau disease gene (VHL).

Richards FM, Latif F, Lerman MI, Zbar B, Maher ER. Richards FM, et al. Among authors: maher er. Hum Mol Genet. 1993 Oct;2(10):1750. doi: 10.1093/hmg/2.10.1750. Hum Mol Genet. 1993. PMID: 7903582 No abstract available.

10

A PCR generated AccI RFLP in the 3' untranslated region of the von Hippel-Lindau disease (VHL) tumour suppressor gene.

Payne SJ, Richards FM, Maher ER. Payne SJ, et al. Among authors: maher er. Hum Mol Genet. 1994 Feb;3(2):390. doi: 10.1093/hmg/3.2.390. Hum Mol Genet. 1994. PMID: 7911705 No abstract available.

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