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Results by year

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

Year Number of Results
1959 2
1960 2
1961 3
1962 1
1963 7
1964 8
1965 9
1966 2
1967 4
1968 5
1969 4
1970 11
1971 4
1972 7
1973 7
1974 16
1975 13
1976 14
1977 17
1978 17
1979 17
1980 13
1981 15
1982 11
1983 13
1984 10
1985 9
1986 6
1987 6
1988 7
1989 17
1990 12
1991 7
1992 4
1993 11
1994 7
1995 7
1996 7
1997 11
1998 12
1999 13
2000 8
2001 12
2002 10
2003 9
2004 14
2005 11
2006 8
2007 9
2008 16
2009 9
2010 13
2011 17
2012 12
2013 12
2014 11
2015 9
2016 17
2017 19
2018 10
2019 24
2020 17
2021 7
2022 9
2023 5

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Article type

Publication date

Search Results

636 results

Results by year

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Page 1
Redefining the Etiologic Landscape of Cerebellar Malformations.
Aldinger KA, Timms AE, Thomson Z, Mirzaa GM, Bennett JT, Rosenberg AB, Roco CM, Hirano M, Abidi F, Haldipur P, Cheng CV, Collins S, Park K, Zeiger J, Overmann LM, Alkuraya FS, Biesecker LG, Braddock SR, Cathey S, Cho MT, Chung BHY, Everman DB, Zarate YA, Jones JR, Schwartz CE, Goldstein A, Hopkin RJ, Krantz ID, Ladda RL, Leppig KA, McGillivray BC, Sell S, Wusik K, Gleeson JG, Nickerson DA, Bamshad MJ, Gerrelli D, Lisgo SN, Seelig G, Ishak GE, Barkovich AJ, Curry CJ, Glass IA, Millen KJ, Doherty D, Dobyns WB. Aldinger KA, et al. Among authors: sell s. Am J Hum Genet. 2019 Sep 5;105(3):606-615. doi: 10.1016/j.ajhg.2019.07.019. Epub 2019 Aug 29. Am J Hum Genet. 2019. PMID: 31474318 Free PMC article.
The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.
Curry CJ, Rosenfeld JA, Grant E, Gripp KW, Anderson C, Aylsworth AS, Saad TB, Chizhikov VV, Dybose G, Fagerberg C, Falco M, Fels C, Fichera M, Graakjaer J, Greco D, Hair J, Hopkins E, Huggins M, Ladda R, Li C, Moeschler J, Nowaczyk MJ, Ozmore JR, Reitano S, Romano C, Roos L, Schnur RE, Sell S, Suwannarat P, Svaneby D, Szybowska M, Tarnopolsky M, Tervo R, Tsai AC, Tucker M, Vallee S, Wheeler FC, Zand DJ, Barkovich AJ, Aradhya S, Shaffer LG, Dobyns WB. Curry CJ, et al. Among authors: sell s. Am J Med Genet A. 2013 Aug;161A(8):1833-52. doi: 10.1002/ajmg.a.35996. Epub 2013 Jun 27. Am J Med Genet A. 2013. PMID: 23813913 Free PMC article.
alpha-Fetoprotein.
Sell S, Becker FF. Sell S, et al. J Natl Cancer Inst. 1978 Jan;60(1):19-26. doi: 10.1093/jnci/60.1.19. J Natl Cancer Inst. 1978. PMID: 75267 Review. No abstract available.
Immunopathology.
Sell S. Sell S. Am J Pathol. 1978 Jan;90(1):211-80. Am J Pathol. 1978. PMID: 23009 Free PMC article. Review. No abstract available.
Circumcision care.
Brown-Trask B, Van Sell S, Carter S, Kindred C. Brown-Trask B, et al. Among authors: van sell s. RN. 2009 Feb;72(2):22-8; quiz 29. RN. 2009. PMID: 19283940 Review.
House calls.
Chime F, Fieldsmith R, Van Sell S, Kindred C, Carter S. Chime F, et al. Among authors: van sell s. RN. 2009 Mar;72(3):22-8; quiz 29. RN. 2009. PMID: 19361058 Review. No abstract available.
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.
Holtz AM, VanCoillie R, Vansickle EA, Carere DA, Withrow K, Torti E, Juusola J, Millan F, Person R, Guillen Sacoto MJ, Si Y, Wentzensen IM, Pugh J, Vasileiou G, Rieger M, Reis A, Argilli E, Sherr EH, Aldinger KA, Dobyns WB, Brunet T, Hoefele J, Wagner M, Haber B, Kotzaeridou U, Keren B, Heron D, Mignot C, Heide S, Courtin T, Buratti J, Murugasen S, Donald KA, O'Heir E, Moody S, Kim KH, Burton BK, Yoon G, Campo MD, Masser-Frye D, Kozenko M, Parkinson C, Sell SL, Gordon PL, Prokop JW, Karaa A, Bupp C, Raby BA. Holtz AM, et al. Among authors: sell sl. Genet Med. 2022 Oct;24(10):2065-2078. doi: 10.1016/j.gim.2022.07.005. Epub 2022 Aug 18. Genet Med. 2022. PMID: 35980381
Tumor markers. Introduction.
Abelev GI, Sell S. Abelev GI, et al. Among authors: sell s. Semin Cancer Biol. 1999 Apr;9(2):61-5. doi: 10.1006/scbi.1998.0088. Semin Cancer Biol. 1999. PMID: 10202128 Review. No abstract available.
636 results