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Article

De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection.

American journal of medical genetics. Part A - 1 Jan 2011

Thevenon Julien, Callier Patrick, Thauvin-Robinet Christel, Mejean Nathalie, Falcon-Eicher Sylvie, Maynadie Marc, de Maistre Emmanuel, Bidot Samuel, Huet Frédéric, Beri-Dexheimer Mylène, Jonveaux Philippe, Mugneret Francine, Faivre Laurence

Abstract excerpt

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Topics

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Share to Abnormalities, Multiple
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 21

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Core Binding Factor Alpha 2 Subunit

Share to Diagnosis, Differential

Share to Intellectual Disability

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Share to Thrombocytopenia

Source

Identifiers

PMID: 21204219
DOI: 10.1002/ajmg.a.33809

Genes

RUNX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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