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

Year Number of Results
1974 1
1978 1
1980 1
1981 1
1982 1
1985 1
1986 2
1987 1
1989 2
1990 3
1991 1
1992 4
1993 4
1994 6
1995 7
1996 8
1997 9
1998 9
1999 4
2000 4
2001 7
2002 5
2003 17
2004 6
2005 4
2006 4
2007 4
2008 7
2009 1
2010 6
2011 2
2012 6
2013 10
2014 4
2015 2
2016 1
2017 1
2018 1
2022 1
2024 0

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Search Results

152 results

Results by year

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Page 1
Peutz-Jeghers syndrome: a systematic review and recommendations for management.
Beggs AD, Latchford AR, Vasen HF, Moslein G, Alonso A, Aretz S, Bertario L, Blanco I, Bülow S, Burn J, Capella G, Colas C, Friedl W, Møller P, Hes FJ, Järvinen H, Mecklin JP, Nagengast FM, Parc Y, Phillips RK, Hyer W, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Tejpar S, Thomas HJ, Wijnen JT, Clark SK, Hodgson SV. Beggs AD, et al. Among authors: hodgson sv. Gut. 2010 Jul;59(7):975-86. doi: 10.1136/gut.2009.198499. Gut. 2010. PMID: 20581245
Fanconi anaemia.
Tischkowitz MD, Hodgson SV. Tischkowitz MD, et al. Among authors: hodgson sv. J Med Genet. 2003 Jan;40(1):1-10. doi: 10.1136/jmg.40.1.1. J Med Genet. 2003. PMID: 12525534 Free PMC article. Review.
Juvenile polyposis.
Desai DC, Neale KF, Talbot IC, Hodgson SV, Phillips RK. Desai DC, et al. Among authors: hodgson sv. Br J Surg. 1995 Jan;82(1):14-7. doi: 10.1002/bjs.1800820106. Br J Surg. 1995. PMID: 7881943 Review.
Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.
Andrews KA, Ascher DB, Pires DEV, Barnes DR, Vialard L, Casey RT, Bradshaw N, Adlard J, Aylwin S, Brennan P, Brewer C, Cole T, Cook JA, Davidson R, Donaldson A, Fryer A, Greenhalgh L, Hodgson SV, Irving R, Lalloo F, McConachie M, McConnell VPM, Morrison PJ, Murday V, Park SM, Simpson HL, Snape K, Stewart S, Tomkins SE, Wallis Y, Izatt L, Goudie D, Lindsay RS, Perry CG, Woodward ER, Antoniou AC, Maher ER. Andrews KA, et al. Among authors: hodgson sv. J Med Genet. 2018 Jun;55(6):384-394. doi: 10.1136/jmedgenet-2017-105127. Epub 2018 Jan 31. J Med Genet. 2018. PMID: 29386252 Free PMC article.
Elongin C (ELOC/TCEB1)-associated von Hippel-Lindau disease.
Andreou A, Yngvadottir B, Bassaganyas L, Clark G, Martin E, Whitworth J, Cornish AJ; Genomics England Research Consortium; Houlston RS, Rich P, Egan C, Hodgson SV, Warren AY, Snape K, Maher ER. Andreou A, et al. Among authors: hodgson sv. Hum Mol Genet. 2022 Aug 23;31(16):2728-2737. doi: 10.1093/hmg/ddac066. Hum Mol Genet. 2022. PMID: 35323939 Free PMC article.
The Johanson-Blizzard syndrome.
Baraitser M, Hodgson SV. Baraitser M, et al. Among authors: hodgson sv. J Med Genet. 1982 Aug;19(4):302-3. doi: 10.1136/jmg.19.4.302. J Med Genet. 1982. PMID: 7120319 Free PMC article.
The genetics of learning disabilities.
Hodgson SV. Hodgson SV. Dev Med Child Neurol. 1998 Feb;40(2):137-40. doi: 10.1111/j.1469-8749.1998.tb15376.x. Dev Med Child Neurol. 1998. PMID: 9489505 Free article. No abstract available.
152 results