A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance (Q56592902)

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A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance
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    A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance (English)
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    John A. Edwards
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    Prahlad K. Sethi
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    Andrew J. Scoma
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    Robin M. Bannerman
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    Lawrence A. Frohman
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    January 1976
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    60
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    1
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    23-32
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