Prenatal diagnosis of trisomy 21 using interphase fluorescencein situ hybridization of post-replicated cells with site-specific cosmid and cosmid contig probes

1995 ◽  
Vol 15 (3) ◽  
pp. 237-248 ◽  
Author(s):  
Ilia V. Soloviev ◽  
Yuri B. Yurov ◽  
Svetlana G. Vorsanova ◽  
Florance Fayet ◽  
Gerard Roizes ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Trisomy 21 ◽  
Fluorescencein Situ Hybridization ◽  
Site Specific ◽  
Cosmid Contig

Fluorescencein situ hybridization with a chromosome 21-specific cosmid contig: 1-day detection of trisomy 21 in uncultured mesenchymal chorionic villus cells

1994 ◽  
Vol 14 (2) ◽  
pp. 87-96 ◽  
Author(s):  
Thue Bryndorf ◽  
Britta Christensen ◽  
Yang Xiang ◽  
John Philip ◽  
Kathy Yokobata ◽  
...  
Keyword(s):  
Trisomy 21 ◽  
Chorionic Villus ◽  
Chromosome 21 ◽  
Fluorescencein Situ Hybridization ◽  
Cosmid Contig

scholarly journals 44 Single-Nucleotide Polymorphisms Expressed by Placental RNA: Assessment for Use in Noninvasive Prenatal Diagnosis of Trisomy 21

2007 ◽  
Vol 53 (12) ◽  
pp. 2223-2224 ◽  
Author(s):  
Attie TJI Go ◽  
Allerdien Visser ◽  
Monique AM Mulders ◽  
Marinus A Blankenstein ◽  
John MG van Vugt ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Single Nucleotide Polymorphisms ◽  
Trisomy 21 ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide ◽  
Noninvasive Prenatal Diagnosis

OP03.10: Prenatal diagnosis vs 1st trimester screening of Trisomy 21 among pregnant women aged 35 or more

2014 ◽  
Vol 44 (S1) ◽  
pp. 70-70
Author(s):  
T. Ghi ◽  
T. Arcangeli ◽  
F. Ravennati ◽  
G. Salsi ◽  
E. Montaguti ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Pregnant Women ◽  
Trisomy 21 ◽  
Trimester Screening

Trisomy 21 in One of Twin Fetuses

PEDIATRICS ◽  
1978 ◽  
Vol 62 (1) ◽  
pp. 52-53
Author(s):  
Richard H. Heller ◽  
Lee S. Palmer
Keyword(s):  
Prenatal Diagnosis ◽  
Trisomy 21 ◽  
Down's Syndrome ◽  
Down’S Syndrome ◽  
Healthy Infant ◽  
The Other ◽  
Technical Problems ◽  
The Family ◽  
Successful Execution

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.

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