Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome

Hum Mol Genet. 1995 Dec;4(12):2417-9. doi: 10.1093/hmg/4.12.2417.

Authors

A Levy¹, S Demczuk, A Aurias, D Depétris, M G Mattei, N Philip

Affiliation

¹ Department of Medicial Genetics, Hôpital d'enfants de la Timone, Paris, France.

PMID: 8634722
DOI: 10.1093/hmg/4.12.2417

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

Chromosome Mapping
Chromosomes, Human, Pair 22*
DiGeorge Syndrome / genetics*
Female
Humans
In Situ Hybridization, Fluorescence
Infant
Sequence Deletion*