A Simple Method for Prenatal Diagnosis of Trisomy 21 on Uncultured Amniocytes

1993 ◽  
Vol 1 (3) ◽  
pp. 245-251 ◽  
Author(s):  
Serge P. Romana ◽  
Gérard Tachdjian ◽  
Luc Druart ◽  
Daniel Cohen ◽  
Roland Berger ◽  
...  
2007 ◽  
Vol 53 (12) ◽  
pp. 2223-2224 ◽  
Author(s):  
Attie TJI Go ◽  
Allerdien Visser ◽  
Monique AM Mulders ◽  
Marinus A Blankenstein ◽  
John MG van Vugt ◽  
...  

2014 ◽  
Vol 44 (S1) ◽  
pp. 70-70
Author(s):  
T. Ghi ◽  
T. Arcangeli ◽  
F. Ravennati ◽  
G. Salsi ◽  
E. Montaguti ◽  
...  

PEDIATRICS ◽  
1978 ◽  
Vol 62 (1) ◽  
pp. 52-53
Author(s):  
Richard H. Heller ◽  
Lee S. Palmer

Both the detection of twins and the successful execution of a double amniocentesis pose significant technical problems in prenatal diagnosis. A case is reported in which one of twin fetuses had trisomy 21 and the other was chromosomally normal. Following counseling, the family chose to continue the pregnancy. At term, the mother was delivered of a healthy infant and a severely macerated fetus with stigmata suggestive of Down's syndrome.


PLoS ONE ◽  
2013 ◽  
Vol 8 (9) ◽  
pp. e74184 ◽  
Author(s):  
Marija Volk ◽  
Aleš Maver ◽  
Luca Lovrečić ◽  
Peter Juvan ◽  
Borut Peterlin

2002 ◽  
Vol 22 (1) ◽  
pp. 29-33 ◽  
Author(s):  
Ingrid Witters ◽  
K. Devriendt ◽  
E. Legius ◽  
G. Matthijs ◽  
D. Van Schoubroeck ◽  
...  

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