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

Year Number of Results
1990 1
1996 3
1997 1
1998 1
1999 2
2000 1
2001 8
2002 8
2003 2
2004 5
2005 2
2006 4
2007 1
2021 0
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38 results
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Page 1
Molecular mechanisms for genomic disorders.
Inoue K, Lupski JR. Inoue K, et al. Annu Rev Genomics Hum Genet. 2002;3:199-242. doi: 10.1146/annurev.genom.3.032802.120023. Epub 2002 Apr 15. Annu Rev Genomics Hum Genet. 2002. PMID: 12142364 Review.
CMT4A: identification of a Hispanic GDAP1 founder mutation.
Boerkoel CF, Takashima H, Nakagawa M, Izumo S, Armstrong D, Butler I, Mancias P, Papasozomenos SC, Stern LZ, Lupski JR. Boerkoel CF, et al. Ann Neurol. 2003 Mar;53(3):400-5. doi: 10.1002/ana.10505. Ann Neurol. 2003. PMID: 12601710
Periaxin mutations cause recessive Dejerine-Sottas neuropathy.
Boerkoel CF, Takashima H, Stankiewicz P, Garcia CA, Leber SM, Rhee-Morris L, Lupski JR. Boerkoel CF, et al. Am J Hum Genet. 2001 Feb;68(2):325-33. doi: 10.1086/318208. Epub 2000 Dec 15. Am J Hum Genet. 2001. PMID: 11133365 Free PMC article.
38 results
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