Two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia: Boucher-Neuhäuser syndrome
Publication year
1997Source
Journal of Medical Genetics, 34, (1997), pp. 761-771ISSN
Publication type
Article / Letter to editor

Display more detailsDisplay less details
Organization
Human Genetics
Ophthalmology
Journal title
Journal of Medical Genetics
Volume
vol. 34
Page start
p. 761
Page end
p. 771
Subject
Hereditary and acquired vitreo-retinal disorders: experimental and clinical research and treatment.; Clinical description and delineation of genetic syndromes; Erfelijke en verworven vitreo-retinale aandoeningen: experimenteel en klinisch onderzoek en behandeling.; Klinische beschrijving en moleculaire definiëring van genetische syndromenThis item appears in the following Collection(s)
- Academic publications [226902]
- Faculty of Medical Sciences [86456]
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.