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Results by year

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

Year Number of Results
1960 1
1964 2
1965 2
1966 1
1967 1
1968 2
1969 1
1970 6
1971 6
1972 6
1973 1
1974 5
1975 10
1976 4
1977 12
1978 1
1979 5
1980 3
1981 1
1982 3
1983 5
1985 9
1986 3
1987 2
1988 6
1989 4
1990 4
1991 1
1992 1
1993 2
1994 3
1996 1
1997 1
1998 1
1999 1
2000 3
2001 5
2002 3
2003 1
2004 1
2005 8
2006 2
2007 9
2008 6
2009 3
2010 5
2011 8
2012 4
2013 9
2014 5
2015 2
2016 3
2017 3
2018 3
2019 5
2020 2
2021 2
2022 2
2023 3
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

207 results

Results by year

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Page 1
Axenfeld-Rieger syndrome: more than meets the eye.
Reis LM, Maheshwari M, Capasso J, Atilla H, Dudakova L, Thompson S, Zitano L, Lay-Son G, Lowry RB, Black J, Lee J, Shue A, Kremlikova Pourova R, Vaneckova M, Skalicka P, Jedlickova J, Trkova M, Williams B, Richard G, Bachman K, Seeley AH, Costakos D, Glaser TM, Levin AV, Liskova P, Murray JC, Semina EV. Reis LM, et al. Among authors: lowry rb. J Med Genet. 2023 Apr;60(4):368-379. doi: 10.1136/jmg-2022-108646. Epub 2022 Jul 26. J Med Genet. 2023. PMID: 35882526 Free PMC article.
Neural tube defects.
Lowry RB. Lowry RB. CMAJ. 2005 Jan 18;172(2):159-60; author reply 160. doi: 10.1503/cmaj.1041670. CMAJ. 2005. PMID: 15655225 Free PMC article. No abstract available.
Tertiary trisomy (22q11q),47,+der(22),t(11;22).
Biederman BM, Lin CC, Lowry RB, Somerville R. Biederman BM, et al. Among authors: lowry rb. Hum Genet. 1980 Feb;53(2):173-7. doi: 10.1007/BF00273491. Hum Genet. 1980. PMID: 7358384
Disease coding systems for arthrogryposis multiplex congenita.
Bedard T, Lowry RB. Bedard T, et al. Among authors: lowry rb. Am J Med Genet C Semin Med Genet. 2019 Sep;181(3):304-309. doi: 10.1002/ajmg.c.31718. Epub 2019 Jun 24. Am J Med Genet C Semin Med Genet. 2019. PMID: 31232506
Genetics in pediatrics.
Lowry RB. Lowry RB. Can Fam Physician. 1988 Apr;34:915-9. Can Fam Physician. 1988. PMID: 21253099 Free PMC article.
Clinical genetics and the Hutterite population: a review of Mendelian disorders.
Boycott KM, Parboosingh JS, Chodirker BN, Lowry RB, McLeod DR, Morris J, Greenberg CR, Chudley AE, Bernier FP, Midgley J, Møller LB, Innes AM. Boycott KM, et al. Among authors: lowry rb. Am J Med Genet A. 2008 Apr 15;146A(8):1088-98. doi: 10.1002/ajmg.a.32245. Am J Med Genet A. 2008. PMID: 18348266 Review.
Familial Poland anomaly.
Lowry RB, Bouvet JP. Lowry RB, et al. J Med Genet. 1983 Apr;20(2):152-4. doi: 10.1136/jmg.20.2.152. J Med Genet. 1983. PMID: 6842555 Free PMC article. No abstract available.
207 results