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- W4295693192 abstract "Holt-Oram syndrome is a rare genetic autosomal dominant disorder which affects the preaxial radial ray of the upper limbs and septation of the heart and/or cardiac conduction. The present article describes the clinical and radiological features of Holt–Oram syndrome in a Tanzanian patient.
 This case emphasises the importance of proper prenatal screening for congenital anomalies and counselling of the parents.
 
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- W4295693192 date "2022-08-10" @default.
- W4295693192 modified "2023-10-14" @default.
- W4295693192 title "Holt-Oram Syndrome; A Case report" @default.
- W4295693192 doi "https://doi.org/10.4314/thrb.v23i2.9" @default.
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