-transparent.png){kind=logo}
Three cases of trisomy 20 mosaicism in amniotic fluid cell cultures are described. Two of the pregnancies resulted in normal full-term infants. The third pregnancy was terminated and revealed a phenotypically normal fetus. A review of five previously reported cases is presented. Explanations of these findings include in vitro nondisjunction, culture of extraembryonic tissue, and true fetal mosaicism. The diagnostic dilemma this presents is discussed.
Related Publications
N B Kardon, and
E Lieber, and
J G Davis, and
L Y Hsu
January 1980,
Zentralblatt fur Gynakologie,
N B Kardon, and
E Lieber, and
J G Davis, and
L Y Hsu
October 1987,
Prenatal diagnosis,
N B Kardon, and
E Lieber, and
J G Davis, and
L Y Hsu
March 1985,
Clinical genetics,
N B Kardon, and
E Lieber, and
J G Davis, and
L Y Hsu
May 1987,
Prenatal diagnosis,
N B Kardon, and
E Lieber, and
J G Davis, and
L Y Hsu
May 2005,
Prenatal diagnosis,
N B Kardon, and
E Lieber, and
J G Davis, and
L Y Hsu
December 2012,
Taiwanese journal of obstetrics & gynecology,
N B Kardon, and
E Lieber, and
J G Davis, and
L Y Hsu
September 2004,
Prenatal diagnosis,
N B Kardon, and
E Lieber, and
J G Davis, and
L Y Hsu
July 2007,
Prenatal diagnosis,
N B Kardon, and
E Lieber, and
J G Davis, and
L Y Hsu
December 2000,
American journal of medical genetics,
N B Kardon, and
E Lieber, and
J G Davis, and
L Y Hsu
January 2003,
Genetic counseling (Geneva, Switzerland),
