F Greenberg, D H Ledbetter. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsCalcitonin/geneticsChildChromosome AberrationsChromosome DeletionChromosomes, Human, Pair 12Face/abnormalitiesHumansPhenotype
Substances: See more » Calcitonin
Year: 1988 PMID: 3189419 DOI: 10.1002/ajmg.1320300423
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299