H F Schuknecht. Show Affiliations »
Abstract
Mesh： See more » Abnormalities, Multiple/embryologyAdolescentAneuploidyBone Diseases, Developmental/embryologyChildChild, PreschoolChromosomes, Human, 13-15Deafness/embryologyEar, Inner/abnormalitiesEar, Inner/embryologyFemaleHumansInfant, NewbornLabyrinth Diseases/embryologyMaleNephritis, Hereditary/embryologyRetinitis Pigmentosa/embryologyTrisomy
Year: 1980 PMID： 7236884
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN： 0547-6844