ABSTRACT In utero interventions are transformative in addressing genetic and anatomic conditions during fetal development. Next generation sequencing enables early genetic testing, playing a pivotal role in prenatal decision‐making by supporting risk stratification, precise and timely diagnosis, which directly informs eligibility for fetal surgical and
Matthew A. Shear +7 more
wiley +1 more source
Quantification of per- and polyfluoroalkyl substances in plasma and follicular fluid of patients undergoing in vitro fertilization in Iowa: A pilot study. [PDF]
Singh-Herren P +5 more
europepmc +1 more source
The effect of in vitro fertilization on the cardiac health of mice. [PDF]
Zhang Z +5 more
europepmc +1 more source
Moderate Diagnostic Yield of Exome Sequencing in Fetal Growth Restriction: Retrospective Insights
ABSTRACT Objective To determine whether invasive genetic testing should be systematically proposed in cases of FGR. Methods Descriptive retrospective study of 159 FGR cases (defined by an estimated fetal growth < 3rd percentile, regardless of Doppler findings) managed at the Toulouse Fetal Medicine Center (TFMC) during 2022–2023.
Maud Langeois +5 more
wiley +1 more source
Complex in vitro fertilization laboratory factors affecting sperm DNA integrity: A narrative review. [PDF]
Vasiee M, Agha-Rahimi A.
europepmc +1 more source
Attitudes Toward Prenatal Interventions in the Fanconi Anemia Community
ABSTRACT Objective In‐utero cell and gene therapies may offer prenatal treatment options for inherited diseases. Preclinical data suggests in‐utero (IU) hematopoietic stem cell transplantation (HSCT) could prevent Fanconi anemia (FA) related bone marrow failure without genotoxic conditioning or immune suppression.
Tony Lum +4 more
wiley +1 more source
Second-trimester pregnancy loss after in vitro fertilization: risk factors and risk reduction. [PDF]
Rubin S +6 more
europepmc +1 more source
From \u3cem\u3eHumanae Vitae\u3c/em\u3e to \u3cem\u3eDonum Vitae\u3c/em\u3e: Symmetry and Consistency in Catholic Biomedical Teaching [PDF]
deLadurantaye, Paul F.
core +1 more source
CUL3‐Related Neurodevelopmental Disorder: Expanding the Prenatal Phenotype
ABSTRACT Objective Pathogenic variants of the CUL3 gene are known to cause a neurodevelopmental disorder with a partially described prenatal phenotype. This study further characterizes and expands the spectrum of prenatal sonographic findings associated with the disorder to improve prenatal diagnosis and counseling.
Yoel Gofin +12 more
wiley +1 more source

