Rapid diagnosis of maternal origin of de novo fetal Robertsonian translocation down syndrome of 46,XY,der(13;21)(q10;q10),+21 by quantitative fluorescent polymerase chain reaction in a pregnancy associated with increased nuchal translucency and an abnormal result of first-trimester maternal serum screening
Author:
Funder
National Science and Technology Council
Publisher
Elsevier BV
Reference3 articles.
1. Unbalanced and balanced heterologous Robertsonian translocations involving chromosome 21 at amniocentesis;Chen;Taiwan J Obstet Gynecol,2010
2. Prenatal diagnosis of 46,XX,der(13;21)(q10;q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites;Chen;Taiwan J Obstet Gynecol,2009
3. Chapter 13: Down syndrome, other full aneuploidies, polyploidy, and the influence of parental age;Gardner,2018
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1. “Not all De novo Robertsonian translocations are truly De novo” - A thought-provoking perspective;Taiwanese Journal of Obstetrics and Gynecology;2024-05
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