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

A de novo insertion, detected prenatally, with normal phenotype.

Journal of medical genetics - 1 May 1992

Hashish A F, Monk N A, Watt A J, Gardner R J

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Aberrations
Share to Chromosomes, Human, Pair 3
Share to Chromosomes, Human, Pair 9
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Karyotyping

Share to Phenotype

Share to Pregnancy

Share to Prenatal Diagnosis

Source

Open in PubMed Open full text

Identifiers

PMID: 1583666
DOI: 10.1136/jmg.29.5.351
PMCID: PMC1015960

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A de novo insertion, detected prenatally, with normal phenotype.PMID 1583666Read ↗

A pediatric genetic disorder diagnosed in adulthood.Semantic proximity Read ↗

Uniparental disomy with normal phenotype.Semantic proximity Read ↗

Genetic causes of abnormal fetal development and inherited disease.Semantic proximity Read ↗

Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations.Semantic proximity Read ↗

Kindler syndrome with a novel mutation and gynaecological complication.Semantic proximity Read ↗

The genetic defect of PNH.Semantic proximity Read ↗

Placental defects are involved in most gene mutations that cause embryonic and fetal death.Semantic proximity Read ↗

Prenatal molecular diagnosis of L1-spectrum disorders.Semantic proximity Read ↗

Complete Trisomy 9 with unusual phenotypic associations.Semantic proximity Read ↗

Genomic analysis of Kabuki syndrome with multiple abnormalities in infancy.Semantic proximity Read ↗

Prenatal diagnosis of Löwe's syndrome: a case report with evidence of de novo mutation.Semantic proximity Read ↗

New genetic findings in old syndromes.Semantic proximity Read ↗

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