J Kunze, E Stephan, M Tolksdorf. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, MultipleAdolescentAdultChildChild, PreschoolChromosome AberrationsChromosome DisordersChromosomes, Human, 16-18Craniofacial Dysostosis/geneticsDeafness/geneticsFemaleHeart Defects, Congenital/geneticsHumansHypotension/geneticsInfantInfant, NewbornKaryotypingMaleMicrocephaly/geneticsMiddle AgedMitosisMuscular Diseases/geneticsPhenotypePsychomotor Disorders/geneticsSyndrome
Year: 1972 PMID: 4565746 DOI: 10.1007/bf00281730
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348