Centric Small Supernumerary Marker Chromosomes
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-20766-2_6
Reference30 articles.
1. Babić I, Brajenović-Milić B, Petrović O, Mustać E, Kapović M (2007) Prenatal diagnosis of complete trisomy 19q. Prenat Diagn 27:644–647
2. Battaglia A (2008) The inv dup (15) or idic (15) syndrome (Tetrasomy 15q). Orphanet J Rare Dis 3:30
3. Dupont JM, Le Tessier D, Baverel F, Rouffet A, Rabineau D (1997) Mosaic isochromosome 20q and normal outcome: a new case ascertained by fluorescence in situ hybridization and a review of the literature. Fetal Diagn Ther 12:283–285
4. Fickelscher I, Starke H, Schulze E, Ernst G, Kosyakova N, Mkrtchyan H, Macdermont K, Sebire N, Liehr T (2007) A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1-evidence for high variability in mosaicism in different tissues of sSMC carriers. Prenat Diagn 27:783–785
5. Fryer AE, Ashworth M, Hawe J, Pilling D, Pauling M, Maye U (2005) Isochromosome 20p associated with multiple congenital abnormalities. Clin Dysmorphol 14:49–50
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