Results 41 to 50 of about 80,804 (125)
Time domain computational modelling of 1D arterial networks in the placenta [PDF]
Published ...
Fisk NM +15 more
core +1 more source
The widespread introduction of molecular genetic research methods into health care practice has made it possible to diagnose rare microdeletion syndromes in patients with multiple congenital malformations..
І. Ластівка +5 more
doaj +1 more source
Abstract Objective We analyzed how anthropometric measures predict cardiometabolic health and how genetic and environmental factors contribute to these associations. Methods Data on 8 indicators of cardiometabolic health, 21 anthropometric measures, and 11 anthropometric indices were available for 216 twin pairs of individuals age 3 to 18 years living ...
Karri Silventoinen +9 more
wiley +1 more source
Congenital diaphragmatic hernia in dizygotic twins [PDF]
Congenital diaphragmatic hernia (CDH) is sometimes seen in siblings but is rarely seen in twins, and five survived cases of CDH in monozygotic or dizygotic twins have been reported in the English literature. Here we report a sixth survived case of CDH in
Ito, Yushi +14 more
core +1 more source
Common knowledge of over a century has it that monozygotic and dizygotic twinning events occur by unrelated mechanisms: monozygotic twinning ‘splits’ embryos, producing anomalously re-arranged embryogenic asymmetries; dizygotic twinning begins with ...
Boklage, Charles E.
core +2 more sources
The efficacy of expanded non‐invasive prenatal testing (NIPT) in a high‐risk twin pregnancies cohort
The efficacy of expanded non‐invasive prenatal testing (NIPT) in twin pregnancies has been less clear. This study presents a relatively optimistic view: expanded NIPT demonstrates high detection rates for common trisomies and moderate DRs for prenatal microdeletion/microduplication syndromes in high‐risk twin pregnancies.
Meng Meng +9 more
wiley +1 more source
Cell‐free DNA test for fetal chromosomal abnormalities in multiple pregnancies
cfDNA testing in twin pregnancies has sufficient screening performance for trisomy 21 but the number of affected cases for other conditions is limited to draw any meaningful conclusion. The use of cfDNA testing in triplet pregnancies and vanishing twins remains an area for further research. Abstract Introduction This study aimed to report the screening
Angel H. W. Kwan +9 more
wiley +1 more source
Monochorionic Twinning in Bioengineered Human Embryo Models
Using a thermoformed‐based microwell platform culture conditions are identified to create human monochorionic twin blastoids from naïve pluripotent stem cells. Twin blastoids form through division of the pluripotent cell mass and implant with higher efficiency than singleton blastoids in a microfluidic endometrium‐on‐chip adhesion assay.
Dorian G. Luijkx +5 more
wiley +1 more source
ABSTRACT Objectives The performance of non‐invasive prenatal screening using cell‐free DNA testing of maternal blood in twin pregnancy is underevaluated, while serum marker‐based strategies yield poor results. This study aimed to assess the performance of non‐invasive prenatal screening for trisomy 21 in twin pregnancy as a first‐tier test.
N. Claudel +21 more
wiley +1 more source
Abstract Aim Genetic influences on cerebral activity have been described previously, but data are scarce in preterms. We aimed to investigate whether a genetic influence causes amplitude‐integrated electroencephalography (aEEG) signals to differ between singletons and twin preterm newborns. Methods This was a retrospective single‐centre study conducted
Christina Schreiner +3 more
wiley +1 more source

