Clinical Genetics · 1984 · 10 citations · 5 references
Life SciencesGeneticsMolecular GeneticsCytogeneticsHuman GeneticsMedical GeneticsChromosomal AbnormalitiesChromosomal DisordersChromosome MappingGenetic DisordersMolecular CytogeneticsMosaicismConstitutional Chromosome AbnormalitiesCytogenetic AbnormalitiesFibroblast CultureInherited Chromosomal DisordersPeptidase ActivityRing Chromosome FormationRing ChromosomesSex Chromosome Mosaicism
A young girl with 46,XX,r(18)/46,XX/45,XX,-18 chromosome constitution is reported. She displays a slight degree of mental retardation. The line with the ring chromosome predominates in blood lymphocytes. In skin fibroblast culture the ring(18) line showed a constant decreasing trend, from 45% at the first passage, down to its disappearance at the 19th passage, where only 46,XX cells were observed. The child/mid parents' ratio of Peptidase A activity in red cells was 0.36. The Peptidase A activity in a fibroblast clone 46,XX,r(18) was 0.55 compared to the 46,XX line. These data suggest that the PEP A locus was lost in ring formation.
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Studies on the quantitative variation of human red cell peptidase A activity
K. P. Sinha, William H. Lewis, G. CORNEY et al. · Annals of Human Genetics · 1970 · 30 citations
Autosomal rings and variable phenotypes
Frederick Hecht, RobertF. Vlietinck · Human Genetics · 1973 · 15 citations