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- W2045131368 abstract "A 3½-year-old retarded girl had multiple congenital anomalies. Cytogenetic analysis revealed a karyotype with a modal number of 2N = 45 and one member of the (21-22) group consistently absent in lymphocytes and skin fibroblasts. The original diagnosis was monosomy G but reanalysis following fluorescence and Giemsa banding techniques demonstrated a translocation involving chromosomes 18 and 21 (45,XX,18-,21-, t[18p21q]). The patient therefore possesses the 18psyndrome and her phenotypic findings are compatible." @default.
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- W2045131368 date "1972-12-01" @default.
- W2045131368 modified "2023-09-27" @default.
- W2045131368 title "An 18p21q Translocation in a Patient With Presumptive Monosomy G" @default.
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- W2045131368 doi "https://doi.org/10.1001/archpedi.1972.02110180110016" @default.
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