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Identification of a novel recessive RELN mutation using a homozygous balanced reciprocal translocation.
Am J Med Genet A. 2007 May 1;143A(9):939-44. doi: 10.1002/ajmg.a.31667.
Am J Med Genet A. 2007.
PMID: 17431900
Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism.
Martin CL, Duvall JA, Ilkin Y, Simon JS, Arreaza MG, Wilkes K, Alvarez-Retuerto A, Whichello A, Powell CM, Rao K, Cook E, Geschwind DH.
Martin CL, et al. Among authors: ilkin y.
Am J Med Genet B Neuropsychiatr Genet. 2007 Oct 5;144B(7):869-76. doi: 10.1002/ajmg.b.30530.
Am J Med Genet B Neuropsychiatr Genet. 2007.
PMID: 17503474
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Diverse fates of paralogs following segmental duplication of telomeric genes.
Wong A, Vallender EJ, Heretis K, Ilkin Y, Lahn BT, Martin CL, Ledbetter DH.
Wong A, et al. Among authors: ilkin y.
Genomics. 2004 Aug;84(2):239-47. doi: 10.1016/j.ygeno.2004.03.001.
Genomics. 2004.
PMID: 15233989
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Molecular definition of an allelic series of mutations disrupting the mouse Lmx1a (dreher) gene.
Chizhikov V, Steshina E, Roberts R, Ilkin Y, Washburn L, Millen KJ.
Chizhikov V, et al. Among authors: ilkin y.
Mamm Genome. 2006 Oct;17(10):1025-32. doi: 10.1007/s00335-006-0033-7. Epub 2006 Oct 3.
Mamm Genome. 2006.
PMID: 17019651
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