Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Prenatal Screening and Diagnosis for Pediatricians

1 Sept 2004

Abstract excerpt

The pediatrician who cares for a child with a birth defect or genetic disorder may be in the best position to alert the family to the possibility of a recurrence of the same or similar problems in future offspring. The family may wish to know about and may benefit from methods that convert probability statements about recurrence risks into more precise knowledge about a specific abnormality in the fetus. The...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Congenital Anomalies and Fetal Surgery
Share to Fetal and Pediatric Neurological Disorders
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 15342871
DOI: 10.1542/peds.2004-1368

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prenatal Screening and Diagnosis for PediatriciansPMID 15342871Read ↗

Prenatal screening for genetic disorders: updated guidelines, proposed counseling, a holistic approach for primary health care providers in developing countriesSemantic proximity Read ↗

The Prenatal Diagnosis of Genetic DiseasesSemantic proximity Read ↗

Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defectsSemantic proximity Read ↗

Screening for Fetal Chromosomal AbnormalitiesSemantic proximity Read ↗

Screening for Fetal Chromosomal AbnormalitiesSemantic proximity Read ↗

Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)Semantic proximity Read ↗

Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)Semantic proximity Read ↗

An overview of current prenatal genetic screening and diagnosis guidelinesSemantic proximity Read ↗

Prenatal diagnosis for chromosome abnormalities: past, present and futureSemantic proximity Read ↗

Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal DiagnosisSemantic proximity Read ↗

Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalitiesSemantic proximity Read ↗

Guideline No. 456: Prenatal Screening for Fetal Chromosomal AnomaliesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.