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

Year Number of Results
1995 2
1996 1
1997 3
1998 3
1999 14
2000 3
2001 3
2002 2
2003 4
2004 11
2005 8
2006 15
2007 21
2008 16
2009 23
2010 25
2011 15
2012 32
2013 25
2014 26
2015 29
2016 23
2017 46
2018 33
2019 31
2020 33
2021 42
2022 35
2023 37
2024 16

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PubMed for id: 482527

500 results

Results by year

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Page 1
Syndromic ciliopathy: a taiwanese single-center study.
Pan YW, Ou TY, Chou YY, Kuo PL, Hsiao HP, Chiu PC, Lin JL, Lo FS, Wang CH, Chen PC, Tsai MC. Pan YW, et al. BMC Med Genomics. 2024 Apr 26;17(1):106. doi: 10.1186/s12920-024-01880-0. BMC Med Genomics. 2024. PMID: 38671463 Free PMC article.
Structurally divergent and recurrently mutated regions of primate genomes.
Mao Y, Harvey WT, Porubsky D, Munson KM, Hoekzema K, Lewis AP, Audano PA, Rozanski A, Yang X, Zhang S, Yoo D, Gordon DS, Fair T, Wei X, Logsdon GA, Haukness M, Dishuck PC, Jeong H, Del Rosario R, Bauer VL, Fattor WT, Wilkerson GK, Mao Y, Shi Y, Sun Q, Lu Q, Paten B, Bakken TE, Pollen AA, Feng G, Sawyer SL, Warren WC, Carbone L, Eichler EE. Mao Y, et al. Cell. 2024 Mar 14;187(6):1547-1562.e13. doi: 10.1016/j.cell.2024.01.052. Epub 2024 Feb 29. Cell. 2024. PMID: 38428424 Free article.
Early prenatal diagnosis of causative homozygous variants in ASCC1 in a fetus with cystic hygroma and additional homozygous variants of unknown significance associated with a neurological phenotype not visible in early gestation: Dual diagnosis or not?
Favier M, Delanne J, Gorincour G, Faivre L, Racine C, Philippe C, Duffourd Y, Vitobello A, Rousseau T, Martz O, Tarris G, Oualiken C, Thauvin-Robinet C, Mau-Them FT. Favier M, et al. Prenat Diagn. 2024 Mar;44(3):352-356. doi: 10.1002/pd.6519. Epub 2024 Feb 11. Prenat Diagn. 2024. PMID: 38342957
500 results