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

Year Number of Results
1990 1
1991 2
1993 4
1997 1
1998 1
1999 1
2000 2
2001 5
2002 8
2003 3
2004 9
2005 5
2006 12
2007 13
2008 19
2009 28
2010 34
2011 22
2012 14
2013 20
2014 21
2015 19
2016 23
2017 15
2018 14
2019 7
2020 19
2021 9
2022 11
2023 7
2024 3

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PubMed for id: 6928

301 results

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Page 1
Prenatal diagnosis and perinatal findings of 17q12 microdeletion encompassing HNF1B in a fetus with bilateral hyperechogenic kidneys on fetal ultrasound and mild renal abnormality after birth, and a review of the literature of prenatal diagnosis of 17q12 microdeletion.
Chen CP, Wu FT, Pan YT, Wu PS, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2024 Jan;63(1):77-80. doi: 10.1016/j.tjog.2023.10.005. Taiwan J Obstet Gynecol. 2024. PMID: 38216274 Free article. Review.
Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions.
Verscaj CP, Velez-Bartolomei F, Bodle E, Chan K, Lyons MJ, Thorson W, Tan WH, Rodig N, Graham JM Jr, Peron A, Quintero-Rivera F, Zackai EH, Thomas MA, Stevens CA, Adam MP, Bird LM, Jones MC, Matalon DR. Verscaj CP, et al. Prenat Diagn. 2024 Feb;44(2):237-246. doi: 10.1002/pd.6424. Epub 2023 Aug 26. Prenat Diagn. 2024. PMID: 37632214 Review.
Elevated level of lysophosphatidic acid among patients with HNF1B mutations and its role in RCAD syndrome: a multiomic study.
Małachowska B, Janikiewicz J, Pietrowska K, Wyka K, Madzio J, Wypyszczak K, Tkaczyk M, Chrul S, Zwiech R, Hogendorf A, Małecki MT, Borowiec M, Krętowski A, Młynarski W, Dobrzyń A, Ciborowski M, Fendler W. Małachowska B, et al. Metabolomics. 2022 Feb 18;18(3):15. doi: 10.1007/s11306-022-01873-z. Metabolomics. 2022. PMID: 35179657 Free PMC article.
301 results