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

Year Number of Results
1980 1
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1984 2
1986 3
1987 3
1989 3
1990 2
1991 9
1992 4
1993 5
1994 6
1995 8
1996 9
1997 5
1998 3
1999 6
2000 5
2001 10
2002 8
2003 8
2004 5
2005 1
2006 4
2007 2
2008 1
2009 3
2010 1
2011 1
2012 3
2013 2
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2017 7
2018 4
2019 5
2020 2
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2024 0

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Similar articles for PMID: 11549681

145 results

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Page 1
Autosomal recessive segregation of a truncating mutation of anti-Müllerian type II receptor in a family affected by the persistent Müllerian duct syndrome contrasts with its dominant negative activity in vitro.
Messika-Zeitoun L, Gouédard L, Belville C, Dutertre M, Lins L, Imbeaud S, Hughes IA, Picard JY, Josso N, di Clemente N. Messika-Zeitoun L, et al. J Clin Endocrinol Metab. 2001 Sep;86(9):4390-7. doi: 10.1210/jcem.86.9.7839. J Clin Endocrinol Metab. 2001. PMID: 11549681
Anti-Müllerian hormone receptor defect.
di Clemente N, Belville C. di Clemente N, et al. Best Pract Res Clin Endocrinol Metab. 2006 Dec;20(4):599-610. doi: 10.1016/j.beem.2006.09.004. Best Pract Res Clin Endocrinol Metab. 2006. PMID: 17161334 Review.
Natural mutations of the anti-Mullerian hormone type II receptor found in persistent Mullerian duct syndrome affect ligand binding, signal transduction and cellular transport.
Belville C, Maréchal JD, Pennetier S, Carmillo P, Masgrau L, Messika-Zeitoun L, Galey J, Machado G, Treton D, Gonzalès J, Picard JY, Josso N, Cate RL, di Clemente N. Belville C, et al. Hum Mol Genet. 2009 Aug 15;18(16):3002-13. doi: 10.1093/hmg/ddp238. Epub 2009 May 20. Hum Mol Genet. 2009. PMID: 19457927
Persistence of Müllerian derivatives in males.
Belville C, Josso N, Picard JY. Belville C, et al. Am J Med Genet. 1999 Dec 29;89(4):218-23. doi: 10.1002/(sici)1096-8628(19991229)89:4<218::aid-ajmg6>3.0.co;2-e. Am J Med Genet. 1999. PMID: 10727997 Review.
145 results