Familial marker chromosome due to 3:1 Disjunction of t(9;15) in a grandparent
- 1 December 1989
- journal article
- research article
- Published by Wiley in Prenatal Diagnosis
- Vol. 9 (12), 851-855
- https://doi.org/10.1002/pd.1970091205
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.This publication has 12 references indexed in Scilit:
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