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Article

[Del(1)(q22-q25) syndrome. Cytogenetics and phenotype].

TSitologiia i genetika - 1 Jan 2000

Zaletaev D V, Dadali E L, Kuleshov N P

Abstract excerpt

A male infant is described with dysmorphology of the head and face, neck, extremities and genitalia, as well as growth and mental retardation and with the de novo interstitial deletion of the proximal segment of the long arm of chromosome 1-del (1) (q22-q25). Comparison of the phenotypic characteristics of this patient with those of previously described patients with similar deletion confirms the existence of the...

Topics

Abnormalities, Multiple
Chromosome Banding
Chromosome Deletion
Chromosomes, Human, Pair 1
Humans
Infant
Karyotyping
Male
Phenotype
Syndrome

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 3617217

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-3617217-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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