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

Year Number of Results
1974 1
1976 2
1977 1
1978 1
1981 1
1982 2
1983 4
1984 1
1987 1
1990 3
1992 2
1993 3
1994 2
1995 3
1996 6
1997 3
1998 4
1999 3
2000 3
2001 3
2002 2
2003 11
2004 5
2005 15
2006 10
2007 9
2008 8
2009 5
2010 7
2011 4
2012 1
2013 2
2014 1
2015 6
2016 3
2017 3
2018 3
2019 3
2020 3
2021 5
2022 3
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Article attribute
Article type
Publication date

Similar articles for PMID: 16691589

154 results
Results by year
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Page 1
Infantile high myopia in Bohring-Opitz syndrome.
Simpson AR, Gibbon CE, Quinn AG, Turnpenny PD. Simpson AR, et al. J AAPOS. 2007 Oct;11(5):524-5. doi: 10.1016/j.jaapos.2007.03.003. Epub 2007 May 10. J AAPOS. 2007. PMID: 17498985
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?
Bohring A, Silengo M, Lerone M, Superneau DW, Spaich C, Braddock SR, Poss A, Opitz JM. Bohring A, et al. Am J Med Genet. 1999 Aug 27;85(5):438-46. doi: 10.1002/(sici)1096-8628(19990827)85:5<438::aid-ajmg2>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10405439 Review.
Three siblings with Robert's syndrome.
Zergollern L, Hitrec F. Zergollern L, et al. Clin Genet. 1976 Apr;9(4):433-6. doi: 10.1111/j.1399-0004.1976.tb02273.x. Clin Genet. 1976. PMID: 177235
Phenotypic spectrum associated with SPECC1L pathogenic variants: new families and critical review of the nosology of Teebi, Opitz GBBB, and Baraitser-Winter syndromes.
Bhoj EJ, Haye D, Toutain A, Bonneau D, Nielsen IK, Lund IB, Bogaard P, Leenskjold S, Karaer K, Wild KT, Grand KL, Astiazaran MC, Gonzalez-Nieto LA, Carvalho A, Lehalle D, Amudhavalli SM, Repnikova E, Saunders C, Thiffault I, Saadi I, Li D, Hakonarson H, Vial Y, Zackai E, Callier P, Drunat S, Verloes A. Bhoj EJ, et al. Eur J Med Genet. 2019 Dec;62(12):103588. doi: 10.1016/j.ejmg.2018.11.022. Epub 2018 Nov 22. Eur J Med Genet. 2019. PMID: 30472488 Free PMC article.
154 results