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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 1
1983 1
1984 2
1985 2
1986 3
1987 4
1988 4
1989 1
1990 1
1991 2
1992 7
1993 11
1994 8
1995 8
1996 11
1997 8
1998 10
1999 18
2000 7
2001 13
2002 9
2003 6
2004 4
2005 3
2006 4
2007 7
2008 2
2009 3
2010 2
2024 0

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159 results

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Page 1
ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer.
Stankovic T, Kidd AM, Sutcliffe A, McGuire GM, Robinson P, Weber P, Bedenham T, Bradwell AR, Easton DF, Lennox GG, Haites N, Byrd PJ, Taylor AM. Stankovic T, et al. Among authors: haites n. Am J Hum Genet. 1998 Feb;62(2):334-45. doi: 10.1086/301706. Am J Hum Genet. 1998. PMID: 9463314 Free PMC article.
Genetic aspects of Charcot-Marie-Tooth disease.
Bell C, Haites N. Bell C, et al. Among authors: haites n. Arch Dis Child. 1998 Apr;78(4):296-300. doi: 10.1136/adc.78.4.296. Arch Dis Child. 1998. PMID: 9623390 Free PMC article. Review. No abstract available.
Online medical genetics resources: a UK perspective.
Stewart A, Haites N, Rose P. Stewart A, et al. Among authors: haites n. BMJ. 2001 Apr 28;322(7293):1037-9. doi: 10.1136/bmj.322.7293.1037. BMJ. 2001. PMID: 11325771 Free PMC article. Review. No abstract available.
Molecular genetics as a 'probe' in ophthalmology.
Haites N. Haites N. Br J Ophthalmol. 1993 Mar;77(3):134-5. doi: 10.1136/bjo.77.3.134. Br J Ophthalmol. 1993. PMID: 8457501 Free PMC article. No abstract available.
Advances in Charcot-Marie-Tooth disease research: cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms. The European CMT Consortium.
Müller HW, Suter U, Van Broeckhoven C, Hanemann CO, Nelis E, Timmerman V, Sancho S, Barrio L, Bolhuis P, Dermietzel R, Frank M, Gabreëls-Festen A, Gillen C, Haites N, Levi G, Mariman E, Martini R, Nave K, Rautenstrauss B, Schachner M, Schenone A, Schneider C, Schröder M, Willecke K. Müller HW, et al. Among authors: haites n. Neurobiol Dis. 1997;4(3-4):215-20. doi: 10.1006/nbdi.1997.0148. Neurobiol Dis. 1997. PMID: 9361297 Review.
Guidelines for follow-up of women at high risk for inherited breast cancer: consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer.
Møller P, Evans G, Haites N, Vasen H, Reis MM, Anderson E, Apold J, Hodgson S, Eccles D, Olsson H, Stoppa-Lyonnet D, Chang-Claude J, Morrison PJ, Bevilacqua G, Heimdal K, Maehle L, Lalloo F, Gregory H, Preece P, Borg A, Nevin NC, Caligo M, Steel CM. Møller P, et al. Among authors: haites n. Dis Markers. 1999 Oct;15(1-3):207-11. doi: 10.1155/1999/920109. Dis Markers. 1999. PMID: 10595280 Free PMC article. Review.
Family communication about genetic risk: the little that is known.
Wilson BJ, Forrest K, van Teijlingen ER, McKee L, Haites N, Matthews E, Simpson SA. Wilson BJ, et al. Among authors: haites n. Community Genet. 2004;7(1):15-24. doi: 10.1159/000080300. Community Genet. 2004. PMID: 15475667 Review.
159 results