A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance
(Q28202255)
scientific article (publication date: 1976)
scientific article (publication date: 1976)
Language:
Current Data About
A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance
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(Q13442814)
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(P304) |
23-32
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(P407) |
(Q1860)
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(P433) |
1
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(P478) |
60
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(P577) |
+1976-01-00T00:00:00Z
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(P921) |
(Q899224)
(Q37525) (Q938107)
(Q2661464)
(Q18967037)
(Q12133)
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(P1433) |
(Q2842959)
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(P1476) |
"A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance" (language: en)
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(P2093) |
J A Edwards
P K Sethi
A J Scoma
R M Bannerman
L A Frohman
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other details
description | scientific article (publication date: 1976) |
External Links
(P356) |
10.1016/0002-9343(76)90547-7
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(P698) |
1251844
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