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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 2
1997 1
2005 1
2007 1
2016 1
2018 1
2020 1
2023 1
2024 2

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PubMed for id: 2288627441

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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.
Maturity-Onset Diabetes of the Young Overview.
Naylor R, Knight Johnson A, del Gaudio D. Naylor R, et al. 2018 May 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. 2018 May 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: 29792621 Free Books & Documents. Review.
17q12 Recurrent Deletion Syndrome.
Mitchel MW, Moreno-De-Luca D, Myers SM, Levy RV, Turner S, Ledbetter DH, Martin CL. Mitchel MW, et al. 2016 Dec 8 [updated 2020 Oct 15]. 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. 2016 Dec 8 [updated 2020 Oct 15]. 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: 27929632 Free Books & Documents. Review.
Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.
Horikawa Y, Iwasaki N, Hara M, Furuta H, Hinokio Y, Cockburn BN, Lindner T, Yamagata K, Ogata M, Tomonaga O, Kuroki H, Kasahara T, Iwamoto Y, Bell GI. Horikawa Y, et al. Nat Genet. 1997 Dec;17(4):384-5. doi: 10.1038/ng1297-384. Nat Genet. 1997. PMID: 9398836 No abstract available.