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

Year Number of Results
1986 2
1988 1
1989 4
1990 1
1991 6
1993 6
1994 4
1995 4
1996 1
1997 3
1998 1
1999 6
2000 1
2001 1
2003 2
2007 1
2008 1
2010 1
2011 1
2012 2
2014 1
2018 1
2019 2
2022 0
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50 results
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Page 1
Siblings with Bohring-Opitz syndrome.
Greenhalgh KL, Newbury-Ecob RA, Lunt PW, Dolling CL, Hargreaves H, Smithson SF. Greenhalgh KL, et al. Among authors: lunt pw. Clin Dysmorphol. 2003 Jan;12(1):15-9. doi: 10.1097/00019605-200301000-00003. Clin Dysmorphol. 2003. PMID: 12514360
The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages.
Jackson L, O'Connor A, Paneque M, Curtisova V, Lunt PW, Pourova RK, Macek M Jr, Stefansdottir V, Turchetti D, Campos M, Henneman L, Godino L, Skirton H, Cornel MC. Jackson L, et al. Among authors: lunt pw. Genet Med. 2019 Mar;21(3):718-726. doi: 10.1038/s41436-018-0132-3. Epub 2018 Jul 27. Genet Med. 2019. PMID: 30050101 Free PMC article.
Diagnostic criteria for facioscapulohumeral muscular dystrophy.
Padberg GW, Lunt PW, Koch M, Fardeau M. Padberg GW, et al. Among authors: lunt pw. Neuromuscul Disord. 1991;1(4):231-4. doi: 10.1016/0960-8966(91)90094-9. Neuromuscul Disord. 1991. PMID: 1822799 No abstract available.
Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics.
Pitceathly RD, Smith C, Fratter C, Alston CL, He L, Craig K, Blakely EL, Evans JC, Taylor J, Shabbir Z, Deschauer M, Pohl U, Roberts ME, Jackson MC, Halfpenny CA, Turnpenny PD, Lunt PW, Hanna MG, Schaefer AM, McFarland R, Horvath R, Chinnery PF, Turnbull DM, Poulton J, Taylor RW, Gorman GS. Pitceathly RD, et al. Among authors: lunt pw. Brain. 2012 Nov;135(Pt 11):3392-403. doi: 10.1093/brain/aws231. Epub 2012 Oct 29. Brain. 2012. PMID: 23107649 Free PMC article.
Prenatal onset spinal muscular atrophy.
MacLeod MJ, Taylor JE, Lunt PW, Mathew CG, Robb SA. MacLeod MJ, et al. Among authors: lunt pw. Eur J Paediatr Neurol. 1999;3(2):65-72. doi: 10.1053/ejpn.1999.0184. Eur J Paediatr Neurol. 1999. PMID: 10700541
50 results