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

Year Number of Results
1993 1
2002 6
2003 3
2004 3
2005 6
2006 1
2007 3
2008 5
2009 3
2010 6
2011 6
2012 5
2013 4
2014 1
2015 3
2016 1
2017 2
2018 2
2019 3
2020 2
2021 5
2022 1
2023 4
2024 0

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66 results

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Page 1
Lymphedema-Distichiasis Syndrome.
Mansour S, Brice GW, Jeffery S, Mortimer P. Mansour S, et al. Among authors: jeffery s. 2005 Mar 29 [updated 2019 Apr 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2005 Mar 29 [updated 2019 Apr 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301630 Free Books & Documents. Review.
Case 9. Hard-to-heal leg ulcer.
McRobert J, Delloson D, Jeffery S. McRobert J, et al. Among authors: jeffery s. J Wound Care. 2023 Dec 1;32(Sup12a):S24-S26. doi: 10.12968/jowc.2023.32.Sup12a.S24. J Wound Care. 2023. PMID: 38175773 No abstract available.
Woundcare4Heroes.
Jeffery S. Jeffery S. Br J Nurs. 2015 Nov 11;24 Suppl 20:S3. doi: 10.12968/bjon.2015.24.Sup20.S3. Br J Nurs. 2015. PMID: 26559234 No abstract available.
Analysis of published PKD1 gene sequence variants.
Gout AM; ADPKD Gene Variant Consortium; Ravine D, Harris PC, Rossetti S, Peters D, Breuning M, Henske EP, Koizumi A, Inoue S, Shimizu Y, Thongnoppakhun W, Yenchitsomanus PT, Deltas C, Sandford R, Torra R, Turco AE, Jeffery S, Fontes M, Somlo S, Furu LM, Smulders YM, Mercier B, Ferec C, Burtey S, Pei Y, Kalaydjieva L, Bogdanova N, McCluskey M, Geon LJ, Wouters CH, Reiterova J, Stekrová J, San Millan JL, Aguiari G, Del Senno L. Gout AM, et al. Among authors: jeffery s. Nat Genet. 2007 Apr;39(4):427-8. doi: 10.1038/ng0407-427. Nat Genet. 2007. PMID: 17392796 Review. No abstract available.
Mutations in EPHB4 cause human venous valve aplasia.
Lyons O, Walker J, Seet C, Ikram M, Kuchta A, Arnold A, Hernández-Vásquez M, Frye M, Vizcay-Barrena G, Fleck RA, Patel AS, Padayachee S, Mortimer P, Jeffery S, Berland S, Mansour S, Ostergaard P, Makinen T, Modarai B, Saha P, Smith A. Lyons O, et al. Among authors: jeffery s. JCI Insight. 2021 Sep 22;6(18):e140952. doi: 10.1172/jci.insight.140952. JCI Insight. 2021. PMID: 34403370 Free PMC article.
Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome.
Ion A, Tartaglia M, Song X, Kalidas K, van der Burgt I, Shaw AC, Ming JE, Zampino G, Zackai EH, Dean JC, Somer M, Parenti G, Crosby AH, Patton MA, Gelb BD, Jeffery S. Ion A, et al. Among authors: jeffery s. Hum Genet. 2002 Oct;111(4-5):421-7. doi: 10.1007/s00439-002-0803-6. Epub 2002 Aug 24. Hum Genet. 2002. PMID: 12384786 Review.
Lipedema: an inherited condition.
Child AH, Gordon KD, Sharpe P, Brice G, Ostergaard P, Jeffery S, Mortimer PS. Child AH, et al. Among authors: jeffery s. Am J Med Genet A. 2010 Apr;152A(4):970-6. doi: 10.1002/ajmg.a.33313. Am J Med Genet A. 2010. PMID: 20358611
66 results