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Page 1
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome.
Beysen D, Raes J, Leroy BP, Lucassen A, Yates JR, Clayton-Smith J, Ilyina H, Brooks SS, Christin-Maitre S, Fellous M, Fryns JP, Kim JR, Lapunzina P, Lemyre E, Meire F, Messiaen LM, Oley C, Splitt M, Thomson J, Van de Peer Y, Veitia RA, De Paepe A, De Baere E. Beysen D, et al. Among authors: ilyina h. Am J Hum Genet. 2005 Aug;77(2):205-18. doi: 10.1086/432083. Epub 2005 Jun 16. Am J Hum Genet. 2005. PMID: 15962237 Free PMC article.
Maternal uniparental disomy 7--review and further delineation of the phenotype.
Kotzot D, Balmer D, Baumer A, Chrzanowska K, Hamel BC, Ilyina H, Krajewska-Walasek M, Lurie IW, Otten BJ, Schoenle E, Tariverdian G, Schinzel A. Kotzot D, et al. Among authors: ilyina h. Eur J Pediatr. 2000 Apr;159(4):247-56. doi: 10.1007/s004310050064. Eur J Pediatr. 2000. PMID: 10789928
Gollop-Wolfgang complex in a 3-month-old girl.
Lurie IW, Ilyina HG. Lurie IW, et al. Among authors: ilyina hg. Am J Med Genet Suppl. 1986;2:191-4. doi: 10.1002/ajmg.1320250623. Am J Med Genet Suppl. 1986. PMID: 3146290 No abstract available.
Familial omphalocele and recurrence risk.
Lurie IW, Ilyina HG. Lurie IW, et al. Among authors: ilyina hg. Am J Med Genet. 1984 Feb;17(2):541-3. doi: 10.1002/ajmg.1320170218. Am J Med Genet. 1984. PMID: 6702903 No abstract available.
Trisomy 2p: analysis of unusual phenotypic findings.
Lurie IW, Ilyina HG, Gurevich DB, Rumyantseva NV, Naumchik IV, Castellan C, Hoeller A, Schinzel A. Lurie IW, et al. Among authors: ilyina hg. Am J Med Genet. 1995 Jan 16;55(2):229-36. doi: 10.1002/ajmg.1320550216. Am J Med Genet. 1995. PMID: 7717424 Review.
14 results