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

Year Number of Results
1965 1
1966 1
1974 1
1977 1
1981 2
1986 1
1993 1
1994 2
1995 1
1996 3
1997 2
1998 2
1999 2
2000 3
2001 5
2002 7
2003 6
2004 4
2005 5
2006 4
2007 9
2008 8
2009 15
2010 10
2011 5
2012 11
2013 18
2014 21
2015 7
2016 9
2017 9
2018 13
2019 21
2020 36
2021 31
2022 29
2023 16
2024 3

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Similar articles for PMID: 29196848

296 results

Results by year

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Page 1
Left-sided congenital heart lesions in mosaic Turner syndrome.
Bouayed Abdelmoula N, Abdelmoula B, Smaoui W, Trabelsi I, Louati R, Aloulou S, Aloulou W, Abid F, Kammoun S, Trigui K, Bedoui O, Denguir H, Mallek S, Ben Aziza M, Dammak J, Kaabi O, Abdellaoui N, Turki F, Kaabi A, Kamoun W, Jabeur J, Ltaif W, Chaker K, Fourati H, M'rabet S, Ben Ameur H, Gouia N, Mhiri MN, Rebai T. Bouayed Abdelmoula N, et al. Mol Genet Genomics. 2018 Apr;293(2):495-501. doi: 10.1007/s00438-017-1398-x. Epub 2017 Dec 1. Mol Genet Genomics. 2018. PMID: 29196848
Low-level 45,X/46,XX mosaicism is not associated with congenital heart disease and thoracic aorta dilatation:prospective magnetic resonance imaging and ultrasound study.
Klásková E, Tüdös Z, Sobek A, Zapletalová J, Dostál J, Zbořilová B, Sobek A Jr, Adamová K, Lattová V, Dostálová Z, Procházka M. Klásková E, et al. Ultrasound Obstet Gynecol. 2015 Jun;45(6):722-7. doi: 10.1002/uog.14627. Epub 2015 May 11. Ultrasound Obstet Gynecol. 2015. PMID: 25042300 Free article.
Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry.
Prakash SK, Bondy CA, Maslen CL, Silberbach M, Lin AE, Perrone L, Limongelli G, Michelena HI, Bossone E, Citro R; BAVCon Investigators, GenTAC Registry Investigators; Lemaire SA, Body SC, Milewicz DM. Prakash SK, et al. Am J Med Genet A. 2016 Dec;170(12):3157-3164. doi: 10.1002/ajmg.a.37953. Epub 2016 Sep 8. Am J Med Genet A. 2016. PMID: 27604636 Free PMC article.
296 results