Results 101 to 110 of about 11,570 (268)

Можливості ультразвукової діагностики хромосомної патології [PDF]

open access: yes, 2016
У статті для оцінки хромосомної патології використовують ультразвукові маркери – комірний простір. Кращий термін вагітності для вимірювання комірцевого простору плодів є від 11 тижнів до 13 тижнів 6 днів.
Антонюк, Ольга Петрівна   +2 more
core  

False negative NIPT results: Risk figures for chromosomes 13,18 and 21 based on chorionic villi results in 5967 cases and literature review [PDF]

open access: yes, 2016
Non-invasive prenatal testing (NIPT) demonstrated a small chance for a false negative result. Since the "fetal" DNA in maternal blood originates from the cytotrophoblast of chorionic villi (CV), some false negative results will have a biological origin ...
Berg, C.D.F. (Cardi) van den   +10 more
core   +1 more source

[Fetal nuchal translucency].

open access: yesGinekologia polska, 2005
In addition to its role in the assessment of risk for trisomy 21, increased nuchal translucency (NT) thickness can also identify a high proportion of other chromosomal defects and is associated with major abnormalities of the heart and great arteries, and a wide range of genetic syndromes.
Kypros H, Nicolaides, Piotr, Wegrzyn
openaire   +1 more source

Relationship Between Fetal Nuchal Thickening and Crown-Rump Length in Thai Fetuses

open access: yesSiriraj Medical Journal, 2008
Objective: To investigate the relationship between the Nuchal thickening (NT) and crown–rump length (CRL) in normal Thai fetuses during 10-14 weeks of gestation. Methods: A prospective observational study was conducted. Ultrasound measurement of NT and
Saifon Chawanpaiboon   +3 more
doaj  

Increased nuchal translucency and distended jugular lymphatic sacs on first‐trimester ultrasound [PDF]

open access: bronze, 2005
M. N. Bekker   +4 more
openalex   +1 more source

OP01.12: Karyotype and outcome of fetuses with increased nuchal translucency above 99th percentile [PDF]

open access: bronze, 2008
Jin Hoon Chung   +5 more
openalex   +1 more source

Aneuploidy screening: Newer noninvasive test gains traction [PDF]

open access: yes, 2016
Favorable results from the 2 studies reviewed here have prompted ACOG to recommend that cell-free DNA screening be discussed with all pregnant patients. Practice changer: Discuss cell-free DNA testing when offering fetal aneuploidy screening to pregnant ...
Farahi, Narges   +3 more
core  

First‐trimester screening for chromosomal abnormalities by integrated application of nuchal translucency, nasal bone, tricuspid regurgitation and ductus venosus flow combined with maternal serum free β‐hCG and PAPP‐A: a 5‐year prospective study [PDF]

open access: bronze, 2011
Saeed Reza Ghaffari   +22 more
openalex   +1 more source

Is there still a role for nuchal translucency measurement in the changing paradigm of first trimester screening? [PDF]

open access: hybrid, 2019
Francesca Bardi   +9 more
openalex   +1 more source

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