Similar articles

• Maternal uniparental isodisomy 11q13qter in a dysmorphic and mentally retarded female with partial trisomy mosaicism 11q13qter.

  Kotzot D, Röthlisberger B, Riegel M, Schinzel A. Kotzot D, et al. J Med Genet. 2001 Dec;38(12):876-81. doi: 10.1136/jmg.38.12.876. J Med Genet. 2001. PMID: 11768394 Free PMC article. No abstract available.
• Genotype/phenotype analysis in a patient with pure and complete trisomy 12p.

  Zumkeller W, Volleth M, Muschke P, Tönnies H, Heller A, Liehr T, Wieacker P, Stumm M. Zumkeller W, et al. Am J Med Genet A. 2004 Sep 1;129A(3):261-4. doi: 10.1002/ajmg.a.30125. Am J Med Genet A. 2004. PMID: 15326625
• Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.

  Chabchoub E, Rodríguez L, Galán E, Mansilla E, Martínez-Fernandez ML, Martínez-Frías ML, Fryns JP, Vermeesch JR. Chabchoub E, et al. J Med Genet. 2007 Apr;44(4):250-6. doi: 10.1136/jmg.2006.045476. Epub 2006 Dec 15. J Med Genet. 2007. PMID: 17172463 Free PMC article.
• [Hypomelanosis of Ito in a girl with Trisomy 13 mosaicism: a cytogenetic study].

  Ronger S, Till M, Kanitakis J, Balme B, Thomas L. Ronger S, et al. Ann Dermatol Venereol. 2003 Nov;130(11):1033-8. Ann Dermatol Venereol. 2003. PMID: 14724538 Review. French.
• Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications.

  Yatsenko SA, Treadwell-Deering D, Krull K, Lewis RA, Glaze D, Stankiewicz P, Lupski JR, Potocki L. Yatsenko SA, et al. Am J Med Genet A. 2005 Oct 1;138A(2):175-80. doi: 10.1002/ajmg.a.30948. Am J Med Genet A. 2005. PMID: 16152635 Review.