• 1 January 1985
    • journal article
    • research article
    • Vol. 28  (4) , 228-230
Abstract
A 5-month-old female patient with psychomotor retardation and minor dysmorphisms is described. Cytogenetic analysis using high-resolution banding technique revealed an interstitial deletion of the short arm of one chromosome 1 (p21 .fwdarw. p22.2) resulting from a de novo translocation t(1;2)(p22;p25).

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