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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
show all 8
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