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Results by year

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

Year Number of Results
1945 2
1946 1
1947 1
1949 2
1950 1
1951 4
1952 5
1953 3
1954 2
1955 1
1957 1
1958 2
1960 1
1962 1
1963 1
1964 1
1965 3
1967 1
1968 2
1969 1
1970 2
1971 1
1972 4
1973 3
1975 1
1976 4
1977 2
1978 2
1979 5
1980 4
1981 4
1982 9
1983 6
1984 6
1985 13
1986 18
1987 10
1988 17
1989 5
1990 5
1991 20
1992 11
1993 7
1994 9
1995 5
1996 15
1997 9
1998 9
1999 17
2000 8
2001 2
2002 5
2003 7
2004 6
2005 4
2006 1
2007 5
2008 6
2009 9
2010 9
2011 15
2012 15
2013 13
2014 11
2015 9
2016 5
2017 8
2018 2
2020 1
2021 1
2022 2
2023 5
2024 1

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Article attribute

Article type

Publication date

Search Results

395 results

Results by year

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Page 1
Hutchinson-Gilford Progeria Syndrome.
Gordon LB, Brown WT, Collins FS. Gordon LB, et al. Among authors: brown wt. 2003 Dec 12 [updated 2023 Oct 19]. 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. 2003 Dec 12 [updated 2023 Oct 19]. 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: 20301300 Free Books & Documents. Review.
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS. Eriksson M, et al. Among authors: brown wt. Nature. 2003 May 15;423(6937):293-8. doi: 10.1038/nature01629. Epub 2003 Apr 25. Nature. 2003. PMID: 12714972 Free PMC article.
PSYCHOGENESIS OF EMESIS.
CLEGHORN RA, BROWN WT. CLEGHORN RA, et al. Among authors: brown wt. Can Psychiatr Assoc J. 1964 Aug;9:299-312. doi: 10.1177/070674376400900405. Can Psychiatr Assoc J. 1964. PMID: 14178679 Review. No abstract available.
The CHARGE association.
Bialer MG, Brown WT. Bialer MG, et al. Among authors: brown wt. J Med Genet. 1990 Aug;27(8):533. doi: 10.1136/jmg.27.8.533. J Med Genet. 1990. PMID: 2213850 Free PMC article. No abstract available.
Corticosteroids and chorea.
Brown WT, Sanberg PR, McGeer PL. Brown WT, et al. Arch Neurol. 1979 Jul;36(7):452-3. doi: 10.1001/archneur.1979.00500430082020. Arch Neurol. 1979. PMID: 156536 No abstract available.
Fragile X targeted pharmacotherapy: lessons learned and future directions.
Erickson CA, Davenport MH, Schaefer TL, Wink LK, Pedapati EV, Sweeney JA, Fitzpatrick SE, Brown WT, Budimirovic D, Hagerman RJ, Hessl D, Kaufmann WE, Berry-Kravis E. Erickson CA, et al. Among authors: brown wt. J Neurodev Disord. 2017 Jun 12;9:7. doi: 10.1186/s11689-017-9186-9. eCollection 2017. J Neurodev Disord. 2017. PMID: 28616096 Free PMC article. Review.
Newborn, carrier, and early childhood screening recommendations for fragile X.
Abrams L, Cronister A, Brown WT, Tassone F, Sherman SL, Finucane B, McConkie-Rosell A, Hagerman R, Kaufmann WE, Picker J, Coffey S, Skinner D, Johnson V, Miller R, Berry-Kravis E. Abrams L, et al. Among authors: brown wt. Pediatrics. 2012 Dec;130(6):1126-35. doi: 10.1542/peds.2012-0693. Epub 2012 Nov 5. Pediatrics. 2012. PMID: 23129072 Review.
Fragile X and autism: a multicenter survey.
Brown WT, Jenkins EC, Cohen IL, Fisch GS, Wolf-Schein EG, Gross A, Waterhouse L, Fein D, Mason-Brothers A, Ritvo E, et al. Brown WT, et al. Am J Med Genet. 1986 Jan-Feb;23(1-2):341-52. doi: 10.1002/ajmg.1320230126. Am J Med Genet. 1986. PMID: 3513570 Review.
395 results