Results 301 to 310 of about 4,096,588 (418)
Prenatal diagnosis of omphalocele with extracorporeal liver. [PDF]
Lestari PM+7 more
europepmc +1 more source
This study demonstrates that the ratio of tNAA to tCr increases during gestation, which correlates with an increase in the number of neurons and cellular energy metabolism in the fetal brain as gestational weeks progress. Additionally, tCho levels exhibit a progressive decrease with advancing gestational weeks, indicating the ongoing development of the
Dejuan Shan+5 more
wiley +1 more source
Chromosomal Microarray Analysis and Karyotype Analysis for Prenatal Diagnosis of Fetuses With Abnormal Ultrasound Soft Markers. [PDF]
Liu L, She L, Zheng Z, Huang S, Wu H.
europepmc +1 more source
Illuminating Immunity: A Systematic Review of Immune Cell Autofluorescence
ABSTRACT Immunophenotyping provides valuable prognostic and diagnostic information, but is technically complex and expensive. The assessment of autofluorescence is label‐free and provides complex information on cell identity. However, research on its application to immunophenotyping has been heterogenous.
Aline Knab+4 more
wiley +1 more source
Prenatal diagnosis of midgut volvulus by fetal MRI: a retrospective study. [PDF]
Kou C, Song Y, Gao D, Zhou L.
europepmc +1 more source
This study mainly to evaluate the performance of nanopore technology in thalassemia detection by utilizing the national genomic reference materials in China. We proved that the reference materials can be used to evaluate the performance of nanopore sequencing in identifying thalassemia mutations, and it's necessary to incorporate triplicates when ...
Xingyu Wei+7 more
wiley +1 more source
B. Holland, J. Myers, C. Woods
semanticscholar +1 more source
Maternal Cell-Free DNA Analysis in a Fetus Affected by Beckwith-Wiedemann Syndrome: Potential for Prenatal Diagnosis. [PDF]
Yamamoto R+4 more
europepmc +1 more source
Chromosome 22q11.2 microdeletion syndrome (22q11.2DS) is a common congenital disorder with high clinical phenotypic heterogeneity. In this study, we retrospectively investigated the incidence of prenatal diagnosis of 22q11.2DS in a single center and summarized its clinical manifestations to expand the phenotypic database ABSTRACT Objective To ...
Jia‐yan Chen+2 more
wiley +1 more source