> Reagents, Molecular Assay, Chromosome Anomaly, Uniparental Disomy
Reagents, Molecular Assay, Chromosome Anomaly, Uniparental Disomy
Definition : Molecular assay reagents intended for use in identifying the abnormal situation in which both members of a chromosome pair are inherited from one parent (i.e., uniparental disomy [UPD]) and the other parent's chromosome for that pair is missing. UPD for some chromosomes is without consequence but, for a few chromosomes, can result in serious conditions including syndromes affecting growth and development. To date, only maternally derived chromosomes 7, 14, and 15 and paternally derived chromosomes 6, 11, 14, and 15 have been shown to have a definite phenotypic effect.
Entry Terms : "Inborn Disorder Diagnostic Reagents" , "Molecular Assay Reagents, Inborn Disorder" , "Uniparental Disomy Detection Reagents" , "Chromosome Anomaly Detection Reagents, Uniparental Disomy" , "Reagents, Molecular Assay, Inborn Disorder, Chromosomal" , "Reagents, Molecular Assay, Inborn Disorder" , "Inborn Disorder Determination Reagents, Chromosomal" , "Inborn Disorder Determination Reagents" , "Chromosomal Inborn Disorder Determination Reagents"
UMDC code : 24030
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