T M Schroeder. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsAnemia, Aplastic/geneticsChromatidsChromosome Aberrations/bloodChromosome DisordersChromosomes, Human, 1-3Chromosomes, Human, 16-18Chromosomes, Human, 19-20Dwarfism/geneticsErythema/geneticsFacial Dermatoses/geneticsHumansKaryotypingLymphocytes/analysisPhotosensitivity Disorders/geneticsSyndromeTelangiectasis/congenital
Year: 1973 PMID: 4757391 DOI: 10.1055/s-0028-1107226
Source DB: PubMed Journal: Dtsch Med Wochenschr ISSN: 0012-0472 Impact factor: 0.628