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

CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy.

Clinical genetics - 1 Feb 2011

Dawson A J, Chernos J, McGowan-Jordan J, Lavoie J, Shetty S, Steinraths M, Wang J-C, Xu J

Abstract excerpt

The aim of this statement is to provide clinicians, cytogeneticists and molecular geneticists of the Canadian College of Medical Geneticists (CCMG) a comprehensive review of the role of UPD in constitutional genetic diagnosis and to provide a guideline as to when investigation for UPD is recommended. Members of the CCMG Cytogenetics, Molecular Genetics, Clinical Practice, and Prenatal Diagnosis committees...

Read the complete abstract on PubMed

Topics

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

Share to Canada
Share to Genetic Testing
Share to Infant, Newborn

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

Share to Neonatal Screening

Share to Pregnancy

Share to Prenatal Diagnosis

Share to Risk Factors

Share to Uniparental Disomy

Source

Identifiers

PMID: 21039433
DOI: 10.1111/j.1399-0004.2010.01547.x

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

CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy.PMID 21039433Read ↗

American College of Medical Genetics Statement on Diagnostic Testing for Uniparental DisomySemantic proximity Read ↗

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

Prenatal Detection of Uniparental Disomies (UPD): Intended and Incidental Finding in the Era of Next Generation GenomicsSemantic proximity Read ↗

Diagnostic testing for uniparental disomy: a points to consider statement from the American College of Medical Genetics and Genomics (ACMG)Semantic proximity Read ↗

Prenatal diagnosis and genetic counseling of uniparental disomySemantic proximity Read ↗

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in CanadaSemantic proximity Read ↗

Clinical and Genomic Approaches for the Diagnosis of Craniofacial Disorders.Semantic proximity Read ↗

Guidelines for molecular karyotyping in constitutional genetic diagnosisSemantic proximity Read ↗

Review disorders of sex development: The evolving role of genomics in diagnosis and gene discovery.Semantic proximity Read ↗

Prenatal testing for uniparental disomy: indications and clinical relevance.Semantic proximity Read ↗

Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patientsSemantic proximity Read ↗

Uniparental disomy and prenatal phenotype: Two case reports and review.Semantic proximity Read ↗

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