J P Fryns, N Logghe, M van Eygen, H Van den Berghe. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsChild, PreschoolChromosome DeletionChromosomes, Human, 6-12 and XExostoses, Multiple Hereditary/geneticsFingers/abnormalitiesHair/abnormalitiesHumansMaleNose/abnormalitiesSyndrome
Year: 1981 PMID: 6974680 DOI: 10.1007/BF00278720
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132