Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 associated with congenital hypoplasia of the tongue and review of the literature
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference24 articles.
1. Small supernumerary marker chromosomes (sSMC) in humans;Liehr;Cyt ogenet Genome Res,2004
2. Molecular cytogenetic and clinical findings in a patient with a small supernumerary r(8) mosaicism;Bettio;Am J Med Genet,2008
3. Mosaicism for a chromosome 8-derived minute marker chromosome in a patient with manifestations of trisomy 8 mosaicism;Spinner;Am J Med Genet,1995
4. Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines;Brecevic;Cyt ogenet Genome Res,2006
5. Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia;Ripperger;Br J Haematol,2011
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1. Paternal UPD14 with sSMC derived from chromosome 14 in Kagami–Ogata syndrome;Chromosome Research;2023-01-19
2. Paternal UPD14 with sSMC derived from chromosome 14 in Kagami-Ogata syndrome;2022-11-18
3. First case of two supernumerary markers derived from chromosome 5 and chromosome 8;Molecular Cytogenetics;2022-06-27
4. Analysis of genetic characteristics of 436 children with dysplasia and detailed analysis of rare karyotype;Open Life Sciences;2022-01-01
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