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

Year Number of Results
1994 1
1997 8
1998 8
1999 9
2000 9
2001 8
2002 10
2003 8
2004 6
2005 8
2006 3
2007 1
2008 4
2009 1
2010 1
2011 1
2012 6
2013 4
2015 5
2016 5
2017 3
2018 5
2019 4
2020 4
2021 2
2022 2
2023 2
2024 0

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Similar articles for PMID: 10193875

121 results

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Page 1
Systematic mutation screening of the pro-opiomelanocortin gene: identification of several genetic variants including three different insertions, one nonsense and two missense point mutations in probands of different weight extremes.
Hinney A, Becker I, Heibült O, Nottebom K, Schmidt A, Ziegler A, Mayer H, Siegfried W, Blum WF, Remschmidt H, Hebebrand J. Hinney A, et al. J Clin Endocrinol Metab. 1998 Oct;83(10):3737-41. doi: 10.1210/jcem.83.10.5298. J Clin Endocrinol Metab. 1998. PMID: 9768693
Mutational analysis of the coding region of the uncoupling protein 2 gene in obese NIDDM patients: impact of a common amino acid polymorphism on juvenile and maturity onset forms of obesity and insulin resistance.
Urhammer SA, Dalgaard LT, Sørensen TI, Møller AM, Andersen T, Tybjaerg-Hansen A, Hansen T, Clausen JO, Vestergaard H, Pedersen O. Urhammer SA, et al. Diabetologia. 1997 Oct;40(10):1227-30. doi: 10.1007/s001250050811. Diabetologia. 1997. PMID: 9349606
121 results