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

Year Number of Results
1982 1
1986 1
1987 1
1990 1
1993 2
1995 1
1996 9
1997 2
1998 1
1999 1
2000 2
2001 3
2002 7
2003 4
2004 5
2005 1
2006 3
2007 2
2008 4
2009 2
2010 3
2011 9
2012 7
2013 9
2014 9
2015 11
2016 8
2017 8
2018 16
2019 20
2020 24
2021 24
2022 31
2023 218
2024 103

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PubMed for id: 743837

500 results

Results by year

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Page 1
Microcystic lymphatic malformations in Turner syndrome are due to somatic mosaicism of PIK3CA.
Nriagu BN, Williams LS, Brewer N, Surrey LF, Srinivasan AS, Li D, Britt A, Treat J, Crowley TB, O'Connor N, Ganguly A, Low D, Queenan M, Drivas TG, Zackai EH, Adams DM, Hakonarson H, Snyder KM, Sheppard SE. Nriagu BN, et al. Am J Med Genet A. 2024 Jan;194(1):64-69. doi: 10.1002/ajmg.a.63385. Epub 2023 Sep 13. Am J Med Genet A. 2024. PMID: 37705207 Free PMC article.
Targeted next-generation sequencing for detection of PIK3CA mutations in archival tissues from patients with Klippel-Trenaunay syndrome in an Asian population : List the full names and institutional addresses for all authors.
Sasaki Y, Ishikawa K, Hatanaka KC, Oyamada Y, Sakuhara Y, Shimizu T, Saito T, Murao N, Onodera T, Miura T, Maeda T, Funayama E, Hatanaka Y, Yamamoto Y, Sasaki S. Sasaki Y, et al. Orphanet J Rare Dis. 2023 Sep 4;18(1):270. doi: 10.1186/s13023-023-02893-1. Orphanet J Rare Dis. 2023. PMID: 37667289 Free PMC article.
500 results