Two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia : Boucher-Neuhäuser syndrome
Publication year
1997Source
Journal of Medical Genetics, 34, 9, (1997), pp. 767-771ISSN
Publication type
Article / Letter to editor

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Organization
Human Genetics
Journal title
Journal of Medical Genetics
Volume
vol. 34
Issue
iss. 9
Page start
p. 767
Page end
p. 771
Subject
Anterior Eye Segment; Eye; Eye Diseases, Hereditary; Neuropathies, Hereditary Sensory and Autonomic; Pigment Epithelium of Eye; Retina; Retinal Diseases; Vitreous BodyThis item appears in the following Collection(s)
- Academic publications [232155]
- Electronic publications [115359]
- Faculty of Medical Sciences [89071]
- Open Access publications [82671]
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