Hexasomy 13q31.3q34 due to two marker chromosomes with inverted duplication in a fetus with increased nuchal translucency

ConclusionA full characterization of small supernumerary marker chromosomes in fetal karyotype is necessary for pregnancy prognosis and genetic counseling. Birth Defects Research (Part A), 2015. © 2015 Wiley Periodicals, Inc.

Source: Birth Defects Research Part A: Clinical and Molecular Teratology - March 1, 2015 Category: Perinatology & Neonatology Authors: Agnieszka Stembalska, Gizela Jagielska, Izabela Laczmanska, Elzbieta Szmida, Alicja Jarczynska, Justyna Gil Tags: Original Research Article Source Type: research