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- W2023097863 abstract "A terminal deletion in the short arm of chromosome 8 was found in a 2.5-year-old boy: 46,XY,del(8) (p22.0) and in a 1-year-old girl: 46,XX,del(8) (p23.1) with dysmorphic craniofacial features and developmental retardation. Erythrocyte GSR activities of the boy and of his parents were within normal limits. Vitamin K dependent coagulation factors in the girl and her parents gave normal results. Clinical findings were compared with previously reported cases and suggested a recognizable syndrome." @default.
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- W2023097863 date "2008-04-23" @default.
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- W2023097863 title "Deficiency of distal 8p -: report of two cases and review of the literature" @default.
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- W2023097863 doi "https://doi.org/10.1111/j.1399-0004.1990.tb04189.x" @default.
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