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

Phenocopy of Wolf-Hirschhorn syndrome in a patient with duplication 12q13.3q14.1.

American journal of medical genetics. Part A - 1 Mar 2009

Dallapiccola Bruno, Bernardini Laura, Novelli Antonio, Mingarelli Rita

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 Abnormalities, Multiple
Share to Chromosomes, Human, Pair 12
Share to Comparative Genomic Hybridization
Share to Cytogenetic Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Duplication

Share to In Situ Hybridization, Fluorescence

Share to Karyotyping

Share to Oligonucleotide Array Sequence Analysis

Source

Identifiers

PMID: 19215045
DOI: 10.1002/ajmg.a.32695

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Phenocopy of Wolf-Hirschhorn syndrome in a patient with duplication 12q13.3q14.1.PMID 19215045Read ↗

Interstitial microduplication 12q13.2-q13.3 in a patient with dysmorphism, developmental delay, atypical seizures and hypospadias: not a phenocopy of Wolf-Hirschhorn syndrome.Semantic proximity Read ↗

Mild Wolf-Hirschhorn phenotype in a girl with unbalanced t(4p;12p) translocation without seizures.Semantic proximity Read ↗

On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.Semantic proximity Read ↗

Wolf-Hirschhorn (4p-) SyndromeSemantic proximity Read ↗

Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome.Semantic proximity Read ↗

109 kb deletion of chromosome 4p16.3 in a patient with mild phenotype of Wolf-Hirschhorn syndrome.Semantic proximity Read ↗

Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map.Semantic proximity Read ↗

Oligomeganephronia in Wolf-Hirschhorn Syndrome.Semantic proximity Read ↗

Wolf-Hirschhorn syndrome: A case series from India.Semantic proximity Read ↗

Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement of FOXG1 appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus.Semantic proximity Read ↗

Wolf-Hirschhorn (4p-) syndrome.Semantic proximity Read ↗

Trisomy 12p and monosomy 4p: phenotype-genotype correlation.Semantic proximity Read ↗

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