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Article

A patient with a de novo 11q24.2-->qter deletion.

Genetic counseling (Geneva, Switzerland) - 1 Jan 2004

Spruijt L, Fryns J P, Hanekom J, Engelen J J, Alofs M, Albrechts J C, Schrander-Stumpel C T

Abstract excerpt

In the group of patients with terminal 11q deletion reported up to now. Jacobson syndrome has been delineated as a distinct clinical entity. In the present report we describe the clinical findings in a 3-year old girl with de novo deletion 11q24.2-->11qter, and compare the findings with Jacobson syndrome.

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Share to Translocation, Genetic
Share to Child, Preschool
Share to Chromosomes, Human, Pair 11

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15083693

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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