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Results by year

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

Year Number of Results
1993 2
2002 1
2003 2
2004 2
2005 1
2006 1
2008 1
2009 1
2011 3
2012 1
2014 1
2015 2
2016 1
2017 3
2018 1
2019 2
2020 1
2021 2
2023 1
2024 0

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PubMed for id: 79867

23 results

Results by year

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Page 1
Two novel TCTN2 mutations cause Meckel-Gruber syndrome.
Zhang M, Chang Z, Tian Y, Wang L, Lu Y. Zhang M, et al. J Hum Genet. 2020 Nov;65(11):1039-1043. doi: 10.1038/s10038-020-0804-0. Epub 2020 Jul 12. J Hum Genet. 2020. PMID: 32655147 Free PMC article.
Joubert Syndrome.
Parisi M, Glass I. Parisi M, et al. 2003 Jul 9 [updated 2017 Jun 29]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2003 Jul 9 [updated 2017 Jun 29]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301500 Free Books & Documents. Review.
Congenital Hepatic Fibrosis Overview ─ RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY.
Gunay-Aygun M, Gahl WA, Heller T. Gunay-Aygun M, et al. 2008 Dec 9 [updated 2014 Apr 24]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2008 Dec 9 [updated 2014 Apr 24]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301743 Free Books & Documents. Review.
23 results