J P Fryns. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdultChromosomes, Human, Pair 6/geneticsChromosomes, Human, Pair 7/geneticsHoloprosencephaly/geneticsHumansIncisor/abnormalitiesMalePhenotypeTranslocation, Genetic
Year: 1998 PMID: 9678712 PMCID: PMC1051378 DOI: 10.1136/jmg.35.7.614
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318