Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype

Small supernumerary marker chromosomes (sSMC) originating from chromosome 10 are rare. Only seven cases have been documented, and among those three cases were diagnosed prenatally. We reported on another prenatal diagnosis of a de novo mosaic sSMC in an apparently normal female fetus whose mother ha...

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Veröffentlicht in:	American journal of medical genetics. Part A 2009-12, Vol.149A (12), p.2768-2774
Hauptverfasser:	Sung, Pi‐Lin, Chang, Sheng‐Ping, Wen, Kuo‐Chang, Chang, Chia‐Ming, Yang, Ming‐Jie, Chen, Lin‐Chao, Chao, Kuan‐Chong, Huang, Chi‐Ying F., Li, Yueh‐Chun, Lin, Chyi‐Chyang
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Biological and medical sciences Chromosome aberrations Chromosome Breakage Chromosomes, Artificial, Bacterial - genetics Chromosomes, Human, Pair 10 - genetics Classical genetics, quantitative genetics, hybrids Female fluorescence in situ hybridization (FISH) Fundamental and applied biological sciences. Psychology Gene Dosage Genetics of eukaryotes. Biological and molecular evolution genome‐wide oligonucleotide microarray Human Humans In Situ Hybridization, Fluorescence marker chromosome 10 Medical genetics Medical sciences Oligonucleotide Array Sequence Analysis Phenotype Polymorphism, Single Nucleotide - genetics Pregnancy small supernumerary marker chromosomes (sSMCs) spectral karyotyping (SKY) trisomy 10p syndrome
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