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

Year Number of Results
1994 1
1999 1
2000 2
2001 3
2002 2
2003 1
2004 3
2005 7
2006 9
2007 4
2008 6
2009 4
2010 9
2011 1
2012 5
2015 1
2016 1
2020 1
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Similar Articles for PMID: 12186176

57 results
Results by year
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Page 1
Genetics 101: detecting mutations in human genes.
Sinclair A. Sinclair A. CMAJ. 2002 Aug 6;167(3):275-9. CMAJ. 2002. PMID: 12186176 Free PMC article. Review. No abstract available.
[Predictive medicine - clinical genetics 2010].
Blum HE. Blum HE. Dtsch Med Wochenschr. 2010 Jun;135(25-26):1334-8. doi: 10.1055/s-0030-1255166. Epub 2010 Jun 16. Dtsch Med Wochenschr. 2010. PMID: 20556694 Review. German. No abstract available.
Development of a high-throughput microarray-based resequencing system for neurological disorders and its application to molecular genetics of amyotrophic lateral sclerosis.
Takahashi Y, Seki N, Ishiura H, Mitsui J, Matsukawa T, Kishino A, Onodera O, Aoki M, Shimozawa N, Murayama S, Itoyama Y, Suzuki Y, Sobue G, Nishizawa M, Goto J, Tsuji S. Takahashi Y, et al. Arch Neurol. 2008 Oct;65(10):1326-32. doi: 10.1001/archneur.65.10.1326. Arch Neurol. 2008. PMID: 18852346
Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP.
Lagarde A, Rouleau E, Ferrari A, Noguchi T, Qiu J, Briaux A, Bourdon V, Rémy V, Gaildrat P, Adélaïde J, Birnbaum D, Lidereau R, Sobol H, Olschwang S. Lagarde A, et al. J Med Genet. 2010 Oct;47(10):721-2. doi: 10.1136/jmg.2010.078964. Epub 2010 Aug 3. J Med Genet. 2010. PMID: 20685668 Free article.
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R. Osborne RJ, et al. Neurology. 2007 Feb 20;68(8):569-77. doi: 10.1212/01.wnl.0000251269.31442.d9. Epub 2006 Dec 6. Neurology. 2007. PMID: 17151338
[Mutational analysis of breast/ovarian cancer hereditary predisposition gene BRCA1 in Tunisian women].
Mestiri S, Monastiri K, Ben Ahmed S, Bouaouina N, Presneau N, Bignon YJ, Khairi H, Chouchane L. Mestiri S, et al. Arch Inst Pasteur Tunis. 2000;77(1-4):11-5. Arch Inst Pasteur Tunis. 2000. PMID: 14658222 French.
Development of a diagnostic genetic test for simplex and autosomal recessive retinitis pigmentosa.
Clark GR, Crowe P, Muszynska D, O'Prey D, O'Neill J, Alexander S, Willoughby CE, McKay GJ, Silvestri G, Simpson DA. Clark GR, et al. Ophthalmology. 2010 Nov;117(11):2169-77.e3. doi: 10.1016/j.ophtha.2010.02.029. Epub 2010 Jun 29. Ophthalmology. 2010. PMID: 20591486
Familial adenomatous polyposis.
Macrae F, du Sart D, Nasioulas S. Macrae F, et al. Best Pract Res Clin Gastroenterol. 2009;23(2):197-207. doi: 10.1016/j.bpg.2009.02.010. Best Pract Res Clin Gastroenterol. 2009. PMID: 19414146 Review.
Zoom-in array comparative genomic hybridization (aCGH) to detect germline rearrangements in cancer susceptibility genes.
Staaf J, Borg A. Staaf J, et al. Methods Mol Biol. 2010;653:221-35. doi: 10.1007/978-1-60761-759-4_13. Methods Mol Biol. 2010. PMID: 20721746 Review.
Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies.
Sherr EH, Owen R, Albertson DG, Pinkel D, Cotter PD, Slavotinek AM, Hetts SW, Jeremy RJ, Schilmoeller G, Schilmoeller K, Wakahiro M, Barkovich AJ. Sherr EH, et al. Neurology. 2005 Nov 8;65(9):1496-8. doi: 10.1212/01.wnl.0000183066.09239.b6. Neurology. 2005. PMID: 16275846
57 results
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