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

Year Number of Results
1991 1
1992 1
1993 1
1994 3
1995 2
1998 2
1999 1
2001 2
2003 3
2004 2
2005 1
2006 3
2007 4
2009 3
2010 3
2011 2
2012 3
2013 5
2014 5
2015 4
2016 6
2017 7
2018 2
2019 5
2020 4
2021 3
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73 results
Results by year
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Page 1
Amelogenesis imperfecta.
Crawford PJ, Aldred M, Bloch-Zupan A. Crawford PJ, et al. Among authors: bloch zupan a. Orphanet J Rare Dis. 2007 Apr 4;2:17. doi: 10.1186/1750-1172-2-17. Orphanet J Rare Dis. 2007. PMID: 17408482 Free PMC article. Review.
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders.
de La Dure-Molla M, Fournier BP, Manzanares MC, Acevedo AC, Hennekam RC, Friedlander L, Boy-Lefèvre ML, Kerner S, Toupenay S, Garrec P, Vi-Fane B, Felizardo R, Berteretche MV, Jordan L, Ferré F, Clauss F, Jung S, de Chalendar M, Troester S, Kawczynski M, Chaloyard J; International Group of Dental Nomenclature, Manière MC, Berdal A, Bloch-Zupan A. de La Dure-Molla M, et al. Among authors: bloch zupan a. Am J Med Genet A. 2019 Oct;179(10):1913-1981. doi: 10.1002/ajmg.a.61316. Epub 2019 Aug 29. Am J Med Genet A. 2019. PMID: 31468724
Hypomorphic mutations of TRIP11 cause odontochondrodysplasia.
Wehrle A, Witkos TM, Unger S, Schneider J, Follit JA, Hermann J, Welting T, Fano V, Hietala M, Vatanavicharn N, Schoner K, Spranger J, Schmidts M, Zabel B, Pazour GJ, Bloch-Zupan A, Nishimura G, Superti-Furga A, Lowe M, Lausch E. Wehrle A, et al. Among authors: bloch zupan a. JCI Insight. 2019 Feb 7;4(3):e124701. doi: 10.1172/jci.insight.124701. Online ahead of print. JCI Insight. 2019. PMID: 30728324 Free PMC article.
Heimler Syndrome.
Mechaussier S, Perrault I, Dollfus H, Bloch-Zupan A, Loundon N, Jonard L, Marlin S. Mechaussier S, et al. Among authors: bloch zupan a. Adv Exp Med Biol. 2020;1299:81-87. doi: 10.1007/978-3-030-60204-8_7. Adv Exp Med Biol. 2020. PMID: 33417209 Review.
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.
Laugel V, Dalloz C, Durand M, Sauvanaud F, Kristensen U, Vincent MC, Pasquier L, Odent S, Cormier-Daire V, Gener B, Tobias ES, Tolmie JL, Martin-Coignard D, Drouin-Garraud V, Heron D, Journel H, Raffo E, Vigneron J, Lyonnet S, Murday V, Gubser-Mercati D, Funalot B, Brueton L, Sanchez Del Pozo J, Muñoz E, Gennery AR, Salih M, Noruzinia M, Prescott K, Ramos L, Stark Z, Fieggen K, Chabrol B, Sarda P, Edery P, Bloch-Zupan A, Fawcett H, Pham D, Egly JM, Lehmann AR, Sarasin A, Dollfus H. Laugel V, et al. Among authors: bloch zupan a. Hum Mutat. 2010 Feb;31(2):113-26. doi: 10.1002/humu.21154. Hum Mutat. 2010. PMID: 19894250
Otodental syndrome.
Bloch-Zupan A, Goodman JR. Bloch-Zupan A, et al. Orphanet J Rare Dis. 2006 Mar 21;1:5. doi: 10.1186/1750-1172-1-5. Orphanet J Rare Dis. 2006. PMID: 16722606 Free PMC article. Review.
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