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

Year Number of Results
1976 1
1987 1
1991 1
1992 1
1994 1
1995 3
1996 4
1997 6
1998 2
1999 3
2000 2
2001 3
2002 3
2004 4
2006 3
2007 4
2008 5
2009 4
2010 3
2011 4
2012 1
2013 3
2014 4
2015 4
2016 3
2017 4
2018 3
2019 4
2020 3
2021 2
2022 4
2023 5
2024 0

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PubMed for id: 325000

88 results

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Page 1
Molecular diagnosis of an infant with TSC2/PKD1 contiguous gene syndrome.
Osumi K, Suga K, Ono A, Goji A, Mori T, Kinoshita Y, Sugano M, Toda Y, Urushihara M, Nakagawa R, Hayabuchi Y, Imoto I, Kagami S. Osumi K, et al. Hum Genome Var. 2020 Jul 16;7:21. doi: 10.1038/s41439-020-0108-0. eCollection 2020. Hum Genome Var. 2020. PMID: 32695431 Free PMC article.
TSC2/PKD1 contiguous gene syndrome, with emphasis on a case with an atypical mild polycystic kidney phenotype and a novel genetic variant.
Reyna-Fabián ME, Alcántara-Ortigoza MA, Hernández-Martínez NL, Berumen J, Jiménez-García R, Gómez-Garza G, González-Del Angel A. Reyna-Fabián ME, et al. Nefrologia (Engl Ed). 2020 Jan-Feb;40(1):91-98. doi: 10.1016/j.nefro.2019.03.003. Epub 2019 Jun 5. Nefrologia (Engl Ed). 2020. PMID: 31176519 Free article. English, Spanish.
[TSC2/PKD1 contiguous gene syndrome. Report of two cases].
Yadaden T, Molinié V, Ples R, Lazure T, Benoît G, Yonneau L, Ferlicot S. Yadaden T, et al. Ann Pathol. 2007 Apr;27(2):136-40. doi: 10.1016/s0242-6498(07)91301-2. Ann Pathol. 2007. PMID: 17909474 French.
TSC2/PKD1 contiguous gene syndrome in an adult.
Culty T, Molinie V, Lebret T, Savareux L, Souid M, Delahousse M, Botto H. Culty T, et al. Minerva Urol Nefrol. 2006 Dec;58(4):351-4. Minerva Urol Nefrol. 2006. PMID: 17268401
88 results