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

Nasal abnormalities in the 9p deletion syndrome.

Archives of otolaryngology--head & neck surgery - 1 Oct 2007

Compadretti Giacomo Ceroni, Tasca Ignazio, Baroncini Anna, Pittalis Maria C

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 Deletion
Share to Chromosome Disorders
Share to Chromosomes, Human, Pair 9
Share to Follow-Up Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to In Situ Hybridization, Fluorescence

Share to Karyotyping

Share to Syndrome

Source

Identifiers

PMID: 17938332
DOI: 10.1001/archotol.133.10.1054

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

Nasal abnormalities in the 9p deletion syndrome.PMID 17938332Read ↗

Fronto-facio-nasal dysplasia in two sisters with additional findings.Semantic proximity Read ↗

Laryngeal abnormalities are frequent in the 22q11 deletion syndromeSemantic proximity Read ↗

Relationship Between the Timing of Fetal Nasal Bone Abnormalities and Fetal Chromosomal Anomalies: A Retrospective Study in a Chinese CohortSemantic proximity Read ↗

Nasal bone assessment in prenatal screening for trisomy 21Semantic proximity Read ↗

Nasal polyposis pathophysiology: Endotype and phenotype open issuesSemantic proximity Read ↗

Nasal bone in first-trimester screening for trisomy 21Semantic proximity Read ↗

Otolaryngological features in a cohort of patients affected with 22q11.2 deletion syndrome: A monocentric survey.Semantic proximity Read ↗

Histopathology of the inner ear in DFNA9.Semantic proximity Read ↗

Clinical phenotypes of polyposis rhinosinusitisSemantic proximity Read ↗

Campomelic dysplasia: airway management in two patients and an update on clinical-molecular correlations in the head and neck.Semantic proximity Read ↗

Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion.Semantic proximity Read ↗

Head and neck manifestations of 22q11.2 deletion syndromesSemantic proximity Read ↗

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