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

Year Number of Results
2007 2
2008 2
2009 5
2010 7
2011 5
2012 7
2013 5
2014 10
2015 13
2016 9
2017 7
2018 9
2019 11
2020 9
2021 17
2022 29
2023 15
2024 0

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Similar articles for PMID: 27234567

137 results

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Page 1
Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome.
Laffargue F, Bourthoumieu S, Llanas B, Baudouin V, Lahoche A, Morin D, Bessenay L, De Parscau L, Cloarec S, Delrue MA, Taupiac E, Dizier E, Laroche C, Bahans C, Yardin C, Lacombe D, Guigonis V. Laffargue F, et al. Arch Dis Child. 2015 Mar;100(3):259-64. doi: 10.1136/archdischild-2014-306810. Epub 2014 Oct 16. Arch Dis Child. 2015. PMID: 25324567
Prenatal diagnosis of HNF1B-associated renal cysts: Is there a need to differentiate intragenic variants from 17q12 microdeletion syndrome?
Vasileiou G, Hoyer J, Thiel CT, Schaefer J, Zapke M, Krumbiegel M, Kraus C, Zweier M, Uebe S, Ekici AB, Schneider M, Wiesener M, Rauch A, Faschingbauer F, Reis A, Zweier C, Popp B. Vasileiou G, et al. Prenat Diagn. 2019 Nov;39(12):1136-1147. doi: 10.1002/pd.5556. Epub 2019 Oct 25. Prenat Diagn. 2019. PMID: 31498910 Free article.
Clinical characteristics of HNF1B-related disorders in a Japanese population.
Nagano C, Morisada N, Nozu K, Kamei K, Tanaka R, Kanda S, Shiona S, Araki Y, Ohara S, Matsumura C, Kasahara K, Mori Y, Seo A, Miura K, Washiyama M, Sugimoto K, Harada R, Tazoe S, Kourakata H, Enseki M, Aotani D, Yamada T, Sakakibara N, Yamamura T, Minamikawa S, Ishikura K, Ito S, Hattori M, Iijima K. Nagano C, et al. Clin Exp Nephrol. 2019 Sep;23(9):1119-1129. doi: 10.1007/s10157-019-01747-0. Epub 2019 May 27. Clin Exp Nephrol. 2019. PMID: 31131422
137 results