J P Fryns. Show Affiliations »
Abstract
Entities: Disease Gene
Mesh: See more » Child, PreschoolChromosome Aberrations/geneticsChromosome DisordersChromosomes, Human, Pair 2Fibromatosis, Gingival/geneticsHumansMaleMultigene Family
Year: 1996 PMID: 9297447
Source DB: PubMed Journal: Ann Genet ISSN: 0003-3995