A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance (Q28202255)
scientific article (publication date: 1976)
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(P31) (Q13442814)
(P304) 23-32
(P407) (Q1860)
(P433) 1
(P478) 60
(P577) +1976-01-00T00:00:00Z
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(Q37525)
(Q938107)
(Q2661464)
(Q18967037)
(Q12133)
(P1433) (Q2842959)
(P1476) "A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance" (language: en)
(P2093) J A Edwards
P K Sethi
A J Scoma
R M Bannerman
L A Frohman
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description scientific article (publication date: 1976)

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