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

Congenital microcephaly detected by prenatal ultrasound: genetic aspects and clinical significance

1 Apr 2000

Abstract excerpt

OBJECTIVE: The aim of this study was to analyze fetuses with prenatally diagnosed microcephaly including the nature of associated anomalies and the genetic-diagnostic implications. DESIGN: Retrospective study design. METHODS: A total of 30 fetuses with reliable dates and with prenatally diagnosed microcephaly as a common feature were analyzed. RESULTS: Microcephaly was diagnosed at a mean gestational age of 28...

Read the complete abstract on PubMed

Topics

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

Share to Fetal and Pediatric Neurological Disorders
Share to Genomic variations and chromosomal abnormalities
Share to Microtubule and mitosis dynamics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 10895445
DOI: 10.1046/j.1469-0705.2000.00092.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Congenital microcephaly detected by prenatal ultrasound: genetic aspects and clinical significancePMID 10895445Read ↗

Small size, big problems: insights and difficulties in prenatal diagnosis of fetal microcephalySemantic proximity Read ↗

Genetic Counseling of Fetal MicrocephalySemantic proximity Read ↗

Genomic and phenotypic delineation of congenital microcephaly.Semantic proximity Read ↗

Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic Microcephaly.Semantic proximity Read ↗

Autosomal Recessive Primary Microcephaly (MCPH): An UpdateSemantic proximity Read ↗

Genetic diagnosis of fetal microcephaly at a single tertiary center in ChinaSemantic proximity Read ↗

[Clinical manifestations and genetics of true microcephaly].Semantic proximity Read ↗

Case Report: Two Cases of Autosomal Recessive Primary Microcephaly Caused by WDR62 Gene MutationSemantic proximity Read ↗

Primary autosomal recessive microcephaly: a novel clinical phenotype.Semantic proximity Read ↗

Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disorders.Semantic proximity Read ↗

Molecular genetics of human microcephaly.Semantic proximity Read ↗

Holoprosencephaly at prenatal diagnosis: analysis of 28 cases regarding etiopathogenic diagnoses.Semantic proximity Read ↗

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