Work

Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR)

Year: 1999

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics

DOI: 10.1002/(sici)1096-8628(19990903)86:1<27::aid-ajmg6>3.0.co;2-7

Authors: Leon McQuade, John Christodoulou, Marcia Budarf, Rani Sachdev, Meredith Wilson, Beverly Emanuel, Alison Colley

Institutions: Children's Hospital at Westmead, The University of Sydney, Children's Hospital of Philadelphia

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Institut National de la Santé et de la Recherche Médicale, National Institutes of Health, National Health and Medical Research Council, National Medical Research Council, National Heart, Lung, and Blood Institute, National Institute on Deafness and Other Communication Disorders

Awards: SCOR IN PEDIATRIC CARDIOVASCULAR DISEASE, VELOCARDIOFACIAL SYNDROME-MOLECULAR AND CLINICAL STUDIES, G4846783882, G7114863532

OpenAlex ID: W2055311846

FWCI: 3.826

Cites: 40

Cited by: 72

Related to: 10