Skip to main content

Some NLM-NCBI services and products are experiencing heavy traffic, which may affect performance and availability. We apologize for the inconvenience and appreciate your patience. For assistance, please contact our Help Desk at info@ncbi.nlm.nih.gov.

American Journal of Human Genetics logoLink to American Journal of Human Genetics
letter
. 1999 Feb;64(2):659–666. doi: 10.1086/302235

A novel 22q11.2 microdeletion in DiGeorge syndrome.

A Rauch, R A Pfeiffer, G Leipold, H Singer, M Tigges, M Hofbeck
PMCID: PMC1377781  PMID: 9973528

Full Text

The Full Text of this article is available as a PDF (1.5 MB).


Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES