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Results by year

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

Year Number of Results
1975 1
1980 1
1988 1
1989 1
1990 1
1992 1
1995 2
1996 1
1997 3
1998 1
2000 1
2001 1
2002 2
2003 3
2004 1
2008 2
2009 2
2010 1
2011 1
2012 2
2013 1
2014 2
2015 2
2016 2
2017 3
2018 1
2019 2
2020 2
2021 4
2022 4
2023 1
2024 0

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PubMed for id: 862747

46 results

Results by year

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Page 1
Co-occurring anomalies in congenital oral clefts.
Stoll C, Alembik Y, Roth MP. Stoll C, et al. Am J Med Genet A. 2022 Jun;188(6):1700-1715. doi: 10.1002/ajmg.a.62689. Epub 2022 Feb 18. Am J Med Genet A. 2022. PMID: 35179301
Congenital heart defects in molecularly confirmed KBG syndrome patients.
Digilio MC, Calcagni G, Gnazzo M, Versacci P, Dentici ML, Capolino R, Sinibaldi L, Baban A, Putotto C, Alfieri P, Unolt M, Lepri FR, Alesi V, Genovese S, Novelli A, Marino B, Dallapiccola B. Digilio MC, et al. Am J Med Genet A. 2022 Apr;188(4):1149-1159. doi: 10.1002/ajmg.a.62632. Epub 2021 Dec 31. Am J Med Genet A. 2022. PMID: 34971082
RASopathies and hemostatic abnormalities: key role of platelet dysfunction.
Di Candia F, Marchetti V, Cirillo F, Di Minno A, Rosano C, Pagano S, Siano MA, Falco M, Assunto A, Boccia G, Magliacane G, Pinna V, De Luca A, Tartaglia M, Di Minno G, Strisciuglio P, Melis D. Di Candia F, et al. Orphanet J Rare Dis. 2021 Dec 2;16(1):499. doi: 10.1186/s13023-021-02122-7. Orphanet J Rare Dis. 2021. PMID: 34857025 Free PMC article.
Single-Cell Transcriptomic Profiling of Vascular Smooth Muscle Cell Phenotype Modulation in Marfan Syndrome Aortic Aneurysm.
Pedroza AJ, Tashima Y, Shad R, Cheng P, Wirka R, Churovich S, Nakamura K, Yokoyama N, Cui JZ, Iosef C, Hiesinger W, Quertermous T, Fischbein MP. Pedroza AJ, et al. Arterioscler Thromb Vasc Biol. 2020 Sep;40(9):2195-2211. doi: 10.1161/ATVBAHA.120.314670. Epub 2020 Jul 23. Arterioscler Thromb Vasc Biol. 2020. PMID: 32698686 Free PMC article.
46 results