J P Fryns. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsChild, PreschoolChromosome DeletionChromosomes, Human, Pair 13Developmental Disabilities/geneticsHeart Septal Defects/geneticsHumansLymphedema/geneticsMaleMicrocephaly/geneticsSyndrome
Year: 1995 PMID: 7545871 DOI: 10.1002/ajmg.1320570332
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299