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Page 1
Terminal 18q deletions are stabilized by neotelomeres.
Guilherme RS, Hermetz KE, Varela PT, Perez AB, Meloni VA, Rudd MK, Kulikowski LD, Melaragno MI. Guilherme RS, et al. Mol Cytogenet. 2015 May 13;8:32. doi: 10.1186/s13039-015-0135-6. eCollection 2015. Mol Cytogenet. 2015. PMID: 25969696 Free PMC article.
Complex small supernumerary marker chromosomes - an update.
Liehr T, Cirkovic S, Lalic T, Guc-Scekic M, de Almeida C, Weimer J, Iourov I, Melaragno MI, Guilherme RS, Stefanou EG, Aktas D, Kreskowski K, Klein E, Ziegler M, Kosyakova N, Volleth M, Hamid AB. Liehr T, et al. Among authors: guilherme rs. Mol Cytogenet. 2013 Oct 31;6:46. doi: 10.1186/1755-8166-6-46. eCollection 2013. Mol Cytogenet. 2013. PMID: 24171835 Free PMC article.
Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion.
Guilherme RS, Soares KC, Simioni M, Vieira TP, Gil-da-Silva-Lopes VL, Kim CA, Brunoni D, Spinner NB, Conlin LK, Christofolini DM, Kulikowski LD, Steiner CE, Melaragno MI. Guilherme RS, et al. Am J Med Genet A. 2014 Jul;164A(7):1659-65. doi: 10.1002/ajmg.a.36512. Epub 2014 Apr 3. Am J Med Genet A. 2014. PMID: 24700634 Review.
Duplication 9p and their implication to phenotype.
Guilherme RS, Meloni VA, Perez AB, Pilla AL, de Ramos MA, Dantas AG, Takeno SS, Kulikowski LD, Melaragno MI. Guilherme RS, et al. BMC Med Genet. 2014 Dec 20;15:142. doi: 10.1186/s12881-014-0142-1. BMC Med Genet. 2014. PMID: 25526829 Free PMC article.
Cytogenomic delineation and clinical follow-up of two siblings with an 8.5 Mb 6q24.2-q25.2 deletion inherited from a paternal insertion.
Meloni VA, Guilherme RS, Oliveira MM, Migliavacca M, Takeno SS, Sobreira NL, de Fatima Faria Soares M, de Mello CB, Melaragno MI. Meloni VA, et al. Among authors: guilherme rs. Am J Med Genet A. 2014 Sep;164A(9):2378-84. doi: 10.1002/ajmg.a.36631. Epub 2014 Jun 4. Am J Med Genet A. 2014. PMID: 24898331 Free PMC article.
25 results