J M Stoler, M Ladoulis, L B Holmes. Show Affiliations »
Abstract
Mesh: See more » Chromosomes, Human, Pair 22Gene DeletionHumansInfant, NewbornLaryngeal Diseases/geneticsLaryngeal Diseases/physiopathologyLarynx/abnormalitiesMale
Year: 1998 PMID: 9741474
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299