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Familial marker chromosome due to 3:1 Disjunction of t(9;15) in a grandparent
Authors:Dr Elizabeth J T Winsor  Margot I van Allen
Institution:Department of Pathology, Toronto General Hospital and Department of Genetics, Hospital for Sick Children, Toronto, Canada
Abstract:An extra small chromosome detected in amniotic fluid was identified as the product of a translocation 46,XX,t(9;15)(p24;q11.2)]. This case is unusual in that individuals with the unbalanced karyotype resulting from a 3:1 disjunction are phenotypically normal.
Keywords:Marker chromosome  3:1 Disjunction  Chromosome 15
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