JB Melo, L Backx, JR Vermeesch, HG Santos… - Journal of applied …, 2011 - Springer Abstract Small supernumerary marker chromosomes (sSMC) are a morphological heterogeneous group of additional abnormal chromosomes that cannot be charac- terized alone by conventional banding cytogenetics. Mo- lecular cytogenetic techniques are valuable tools for the ... -
RD Burnside, J Ibrahim, C Flora… - Cytogenetic and …, 2011 - content.karger.com ...Chromosome analysis of the phenotypically normal father revealed the same deleted chromosome 8, as well as an apparently balancing mosaic markerchromosome 8. FISH studies revealed that the majority of the chromosome 8 alpha-satellite DNA resided in the marker... -
C Eckmann-Scholz, H Tönnies… - Journal of Maternal …, 2011 - informahealthcare.com Introduction. We report on a prenatally diagnosed de novo small supernumerary marker chromosome (sSMC) derived form chromosome 18. Molecular cytogenetic studies led to information about the clinical relevance of the sSMC-induced chromosomal imbalance. As prenatal ... -
X Chen, G Raca, J Laffin, KN Babaian… - Journal of …, 2011 - Am Soc Andrology ... Key words: Male infertility, hypogonadism, genetic abnormalities, ring Y chromosomes, supernumerary markerchromosome, AZF regions. Structural ... (B–C) Partial karyograms showing markerchromosome next to chromosome 15. (B ... -
S Yakut, Z Cetin, S Berker-Karauzum… - Genetic counseling ( …, 2011 - ncbi.nlm.nih.gov We report here a prenatal case with de novo supernumerary marker chromosome originating from chromosome 17 in non-mosaic form resulting in normal pregnancy outcome. In this case, a 26-year-old pregnant woman was referred for amniocenthesis and microdeletion ...
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