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Developmental Presentation of 22q11.2 Deletion (DiGeorge/Velocardiofacial Syndrome)

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Year: 1998
Type: article
Source: Journal of Developmental & Behavioral Pediatrics
DOI: 10.1097/00004703-199810000-00004
Authors: PAUL P. WANG, CYNTHIA SOLOT, EDWARD M. MOSS, MARSHA GERDES, DONNA M. McDONALD-McGINN, DEBORAH A. DRISCOLL, BEVERLY S. EMANUEL, ELAINE H. ZACKAI
Institutions: Children's Hospital of Philadelphia, University of Pennsylvania
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: National Institute on Deafness and Other Communication Disorders, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: VELOCARDIOFACIAL SYNDROME-MOLECULAR AND CLINICAL STUDIES, NEUROPSYCHOLOGY OF WORKING MEMORY IN GENETIC SYNDROMES
OpenAlex ID: W2329401245
FWCI: 1.26
Cites:
Cited by: 28
Related to: 10
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