J P Fryns, A Kleczkowska, H van den Berghe. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsAdultChromosomes, Human, Pair 15Chromosomes, Human, Pair 22Facial Bones/abnormalitiesFemaleFrontal Bone/abnormalitiesHumansHypertelorism/geneticsNasal Bone/abnormalitiesStrabismus/geneticsTranslocation, Genetic
Year: 1993 PMID: 8403454 DOI: 10.1111/j.1399-0004.1993.tb03841.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438