Results 301 to 310 of about 797,428 (374)

Yield of Whole Genome Sequencing for Pathogenic Single Nucleotide Variants in Congenital Heart Disease: A Systematic Review and Meta‐Analysis

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa   +7 more
wiley   +1 more source

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.

open access: yesAmerican Journal of Human Genetics, 2019
Z. Dong   +38 more
semanticscholar   +1 more source

Recurrent Miscarriage: A Review [PDF]

open access: yesReproductive Medicine, Gynecology & Obstetrics, 2017
openaire   +1 more source

The Expanding Role of Gene Sequencing in Shaping Fetal Therapies: Clinical and Ethical Considerations

open access: yesPrenatal Diagnosis, EarlyView.
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

Sex‐specific associations between hypertensive disorders in pregnancy and fetal and placental weight

open access: yesPediatric Investigation, EarlyView.
In a US birth cohort, males of mothers with gestational hypertension had higher birthweight Z‐scores, but this association was not found among females. For the fetoplacental weight ratio, any hypertensive disorders during pregnancy were associated with a lower ratio among females only.
Alexandra R. Sitarik   +5 more
wiley   +1 more source

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