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- W1997975286 abstract "A boy with severe growth and psychomotor retardation, facial dysmorphism, a large atrial septal defect, limitation of joint movement and hearing impairment is described. High-resolution banding chromosome analysis showed interstitial deletion of the proximal segment of chromosome 3: 46, XY, del(3)(p12p14.2) de novo. The deleted chromosome 3 was of paternal origin as judged from Q-banding polymorphisms. Delineation of proximal 3p deletion syndrome is proposed by summarizing the clinical and cytogenetical findings of the present and previously reported five patients." @default.
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- W1997975286 date "1988-02-01" @default.
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- W1997975286 title "Proximal 3p Deletion: Case Report and Review of the Literature" @default.
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- W1997975286 doi "https://doi.org/10.1111/j.1442-200x.1988.tb02501.x" @default.
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