Related Experiment Videos
Current status of first trimester fetal diagnosis of genetic diseases
Human Reproduction (Oxford, England)
|August 1, 1986
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Ethical guidance on human embryonic and fetal tissue transplantation: a European overview.
Medicine, health care, and philosophy·2002
Outcome of first-trimester chorionic villus sampling for genetic investigation in multiple pregnancy.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2001
RhD genotyping by quantitative fluorescent polymerase chain reaction: a new approach.
BJOG : an international journal of obstetrics and gynaecology·2001
Improvement in outcomes of multifetal pregnancy reduction with increased experience.
American journal of obstetrics and gynecology·2001
Selective termination for structural, chromosomal, and mendelian anomalies: international experience.
American journal of obstetrics and gynecology·1999
Virulent bacterial pathogens disassemble the epididymal amyloid matrix to evade host defense.
Human reproduction (Oxford, England)·2026
Endometrial scratching in patients with unexplained infertility who have a good prognosis for natural conception: a randomized controlled trial (SCRaTCH-OFO).
Human reproduction (Oxford, England)·2026
The two-shot protocol. A randomized controlled trial of a novel two-injection ovarian stimulation strategy.
Human reproduction (Oxford, England)·2026
Birthweight trends for babies born using Assisted Reproductive Treatments between 1991 and 2018: a national cohort study.
Human reproduction (Oxford, England)·2026
Interindividual variability of sperm DNA methylation is associated with reduced fecundability in couples attempting natural conception.
Human reproduction (Oxford, England)·2026
Caregiver's perspectives toward genome sequencing in children with neurodevelopmental disorders: Integrating genomic information into pediatric care.
Current problems in pediatric and adolescent health care·2026
Father and son with a pathogenic variant c.614dup p.(Gln206Thrfs*20) in the NR5A1 gene: a case report.
Frontiers in pediatrics·2026
Pediatric Spinal Cord Astrocytoma With Granular Cell-Like Morphology and KIAA1549::BRAF Fusion.
Neuropathology : official journal of the Japanese Society of Neuropathology·2026
KCTD1 p.Gly62Asp Variant in Scalp-Ear-Nipple Syndrome: Phenotypic and Structural Insights.
The Journal of craniofacial surgery·2026
Schizophrenia-associated polygenic liability and structural genomic risk demonstrate broadly distributed neuropsychiatric associations in the All of Us Research Program.
medRxiv : the preprint server for health sciences·2026