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Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome.
Gothelf D, Presburger G, Zohar AH, Burg M, Nahmani A, Frydman M, Shohat M, Inbar D, Aviram-Goldring A, Yeshaya J, Steinberg T, Finkelstein Y, Frisch A, Weizman A, Apter A. Gothelf D, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 Apr 1;126B(1):99-105. doi: 10.1002/ajmg.b.20124. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15048657
Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24.
Abu A, Frydman M, Marek D, Pras E, Stolovitch C, Aviram-Goldring A, Rienstein S, Reznik-Wolf H, Pras E. Abu A, et al. Among authors: aviram goldring a. Invest Ophthalmol Vis Sci. 2006 Dec;47(12):5283-7. doi: 10.1167/iovs.06-0206. Invest Ophthalmol Vis Sci. 2006. PMID: 17122114
Preimplantation genetic haplotyping a new application for diagnosis of translocation carrier's embryos- preliminary observations of two robertsonian translocation carrier families.
Shamash J, Rienstein S, Wolf-Reznik H, Pras E, Dekel M, Litmanovitch T, Brengauz M, Goldman B, Yonath H, Dor J, Levron J, Aviram-Goldring A. Shamash J, et al. Among authors: aviram goldring a. J Assist Reprod Genet. 2011 Jan;28(1):77-83. doi: 10.1007/s10815-010-9483-7. Epub 2010 Sep 25. J Assist Reprod Genet. 2011. PMID: 20872064 Free PMC article.
Screening of human pluripotent stem cells using CGH and FISH reveals low-grade mosaic aneuploidy and a recurrent amplification of chromosome 1q.
Dekel-Naftali M, Aviram-Goldring A, Litmanovitch T, Shamash J, Reznik-Wolf H, Laevsky I, Amit M, Itskovitz-Eldor J, Yung Y, Hourvitz A, Schiff E, Rienstein S. Dekel-Naftali M, et al. Among authors: aviram goldring a. Eur J Hum Genet. 2012 Dec;20(12):1248-55. doi: 10.1038/ejhg.2012.128. Epub 2012 Jun 20. Eur J Hum Genet. 2012. PMID: 22713809 Free PMC article.
31 results