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

Year Number of Results
1991 1
1992 1
2000 2
2001 2
2003 2
2004 1
2005 1
2006 1
2007 2
2008 3
2009 2
2010 2
2011 1
2012 1
2024 0

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Page 1
TFAP2A mutations result in branchio-oculo-facial syndrome.
Milunsky JM, Maher TA, Zhao G, Roberts AE, Stalker HJ, Zori RT, Burch MN, Clemens M, Mulliken JB, Smith R, Lin AE. Milunsky JM, et al. Among authors: maher ta. Am J Hum Genet. 2008 May;82(5):1171-7. doi: 10.1016/j.ajhg.2008.03.005. Am J Hum Genet. 2008. PMID: 18423521 Free PMC article.
Prenatal molecular diagnosis of tuberous sclerosis complex.
Milunsky A, Ito M, Maher TA, Flynn M, Milunsky JM. Milunsky A, et al. Among authors: maher ta. Am J Obstet Gynecol. 2009 Mar;200(3):321.e1-6. doi: 10.1016/j.ajog.2008.11.004. Am J Obstet Gynecol. 2009. PMID: 19254590
LADD syndrome is caused by FGF10 mutations.
Milunsky JM, Zhao G, Maher TA, Colby R, Everman DB. Milunsky JM, et al. Among authors: maher ta. Clin Genet. 2006 Apr;69(4):349-54. doi: 10.1111/j.1399-0004.2006.00597.x. Clin Genet. 2006. PMID: 16630169
Mutation analysis in Rett syndrome.
Milunsky JM, Lebo RV, Ikuta T, Maher TA, Haverty CE, Milunsky A. Milunsky JM, et al. Among authors: maher ta. Genet Test. 2001 Winter;5(4):321-5. doi: 10.1089/109065701753617462. Genet Test. 2001. PMID: 11960578
22 results