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2005 | 1 |
2006 | 1 |
2010 | 1 |
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Recurrent inversion events at 17q21.31 microdeletion locus are linked to the MAPT H2 haplotype.
Cytogenet Genome Res. 2010;129(4):275-9. doi: 10.1159/000315901. Epub 2010 Jul 6.
Cytogenet Genome Res. 2010.
PMID: 20606400
Free PMC article.
Chromosome 19p13 loci in Finnish migraine with aura families.
Kaunisto MA, Tikka PJ, Kallela M, Leal SM, Papp JC, Korhonen A, Hämäläinen E, Harno H, Havanka H, Nissilä M, Säkö E, Ilmavirta M, Kaprio J, Färkkilä M, Ophoff RA, Palotie A, Wessman M.
Kaunisto MA, et al.
Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):85-9. doi: 10.1002/ajmg.b.30082.
Am J Med Genet B Neuropsychiatr Genet. 2005.
PMID: 15449251
Free PMC article.
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Accommodating chromosome inversions in linkage analysis.
Chen GK, Slaten E, Ophoff RA, Lange K.
Chen GK, et al.
Am J Hum Genet. 2006 Aug;79(2):238-51. doi: 10.1086/505540. Epub 2006 Jun 6.
Am J Hum Genet. 2006.
PMID: 16826515
Free PMC article.
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