Results 151 to 160 of about 24,363 (274)

A review of evidence on non-invasive prenatal diagnosis (NIPD) : tests for fetal RHD genotype [PDF]

open access: yes, 2007
This report concentrates on three main areas. First and foremost, we set the background context for RhD NIPD in prenatal care. While the methodology chapter describes how the literature review was carried out and how additional information was collected,
Clay, Diane   +5 more
core  

Impact of double versus single blastocyst biopsy and vitrification on clinical and neonatal outcomes in PGT cycles: A systematic review and meta‐analysis of embryo retesting

open access: yesActa Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 1, Page 30-49, January 2026.
Rebiopsied and revitrified blastocysts may be linked to lower pregnancy and live birth rates in single euploid frozen embryo transfer cycles (very low‐quality evidence). Subgroup effects by biopsy day and morphology may hold clinical relevance and guide future study design.
Alessandra A. Vireque   +4 more
wiley   +1 more source

Pregnancy and perinatal outcomes after day 5 versus day 6 blastocyst‐stage embryo transfer: A systematic review and meta‐analysis

open access: yesActa Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 1, Page 50-69, January 2026.
We conducted a meta‐analysis to compare the pregnancy and perinatal outcomes after day 5 versus day 6 single frozen‐thawed blastocyst transfer, aims to identify more appropriate strategies for transplantation. ART practitioners should give priority to transfer D5 rather than D6 blastocysts in single vitrified‐warmed cycle in clinical practice. Abstract
Wenhui Hou   +6 more
wiley   +1 more source

Evaluating the Clinical Utility of Genomic Sequencing After Perinatal Death

open access: yesClinical Genetics, Volume 109, Issue 1, Page 109-121, January 2026.
Genomic sequencing after perinatal death is shown to provide meaningful improvements in counselling, recurrence risk estimation, and family planning—even when a genetic diagnosis is not found. ABSTRACT Following termination of pregnancy for fetal anomaly or unexplained perinatal death (PND), clinical geneticists advise on possible genetic causes and ...
Camille M. Schubert   +102 more
wiley   +1 more source

Chromosomal, gestational, and neonatal outcomes of embryos classified as a mosaic by preimplantation genetic testing for aneuploidy [PDF]

open access: bronze, 2023
Manuel Viotti   +24 more
openalex   +1 more source

Preimplantation genetic testing for a new abnormal cleavage behavior

open access: yesAsian Journal of Andrology, 2021
Ming-Zhao Li   +3 more
doaj   +1 more source

Preimplantation Genetic Testing within the Public Healthcare System in Slovenia

open access: yesBalkan Journal of Medical Genetics
Preimplantation genetic testing (PGT) is the earliest form of prenatal diagnosis that has become an established procedure for couples at risk of passing a severe genetic disease to their offspring.
Volk M   +10 more
doaj   +1 more source

Mutations in UMOD Contribute to the Pathogenesis of ADTKD‐UMOD by Influencing the Function of Complement Factor H

open access: yesJournal of Cellular and Molecular Medicine, Volume 30, Issue 2, January 2026.
ABSTRACT Tubular atrophy and interstitial fibrosis are basic renal pathological changes in autosomal dominant tubulointerstitial kidney disease (ADTKD). Reduced secretion or abnormal structure of uromodulin (UMOD) are recognised pathogenic factors of ADTKD.
Qiuyu Xie   +4 more
wiley   +1 more source

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