Journal of Medical Genetics · 1974 · 38 citations · 4 references
Life SciencesGeneticsMolecular GeneticsCytogeneticsHuman GeneticsPediatric GeneticsChromosomal AbnormalitiesChromosomal DisordersChromosomal TranslocationsClinical CytogeneticsNumerical Chromosome AbnormalitiesStructural Chromosome AbnormalitiesChromosomal Translocation AnalysisConstitutional Chromosome AbnormalitiesCytogenetic AbnormalitiesFetal Chromosomal AbnormalitiesInherited Chromosomal TranslocationsParental Chromosomal AbnormalitiesTranslocation Syndromes
Cytogenetic studies of an infant with malformations and a peculiar appearance showed a partial trisomy of chromosome 12. The mother carried a translocation of the distal part of chromosome 12 onto the short arm of chromosome 21, with breakpoints most likely at 12q24 and 21p11.
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Identification of human chromosomes by DNA-binding fluorescent agents
T. Caspersson, L. Zech, C. Johansson et al. · Chromosoma · 1970 · 980 citations
[Partial 7q trisomy due to t(7;12) (q22;q24) familial translocation].
S. Carpentier, Rethoré Mo, J Lejeune · PubMed · 1972 · 13 citations