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

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly

5 Oct 2021

Abstract excerpt

BACKGROUND: This study aimed to delineate the clinical phenotype of patients with 9p deletions, pinpoint the chromosomal breakpoints, and identify the critical region for trigonocephaly, which is a frequent finding in 9p terminal deletion. METHODS: We investigated a cohort of nine patients with chromosome 9p terminal deletions who all displayed developmental delay, intellectual disability, hypotonia, and...

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 Hedgehog Signaling Pathway Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34609792
DOI: 10.1002/mgg3.1829

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

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephalyPMID 34609792Read ↗

Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype.Semantic proximity Read ↗

Using a new analytic approach for genotyping and phenotyping chromosome 9p deletion syndrome.Semantic proximity Read ↗

Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9p.Semantic proximity Read ↗

Chromosome 9p deletion syndrome and sex reversal: Novel findings and redefinition of the critically deleted regionsSemantic proximity Read ↗

Molecular and cytogenetic characterization of 9p– abnormalitiesSemantic proximity Read ↗

Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly.Semantic proximity Read ↗

Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review.Semantic proximity Read ↗

Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations.Semantic proximity Read ↗

Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases.Semantic proximity Read ↗

Axenfeld-Rieger anomaly and Axenfeld-Rieger syndrome: clinical, molecular-cytogenetic, and DNA array analyses of three patients with chromosomal defects at 6p25.Semantic proximity Read ↗

A terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four-generation family.Semantic proximity Read ↗

A cryptic unbalanced translocation t(2;9)(p25.2;q34.3) causes the phenotype of 9q subtelomeric deletion syndrome and additional exophthalmos and joint contractures.Semantic proximity Read ↗

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