Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
Publication year
2000Source
European Journal of Paediatric Neurology, 4, (2000), pp. 39-43ISSN
Publication type
Article / Letter to editor

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Organization
Neurology
Human Genetics
Journal title
European Journal of Paediatric Neurology
Volume
vol. 4
Page start
p. 39
Page end
p. 43
Subject
(Fragile) breakage-prone sites in human chromosomes; Clinical description and delineation of genetic syndromes; Pathophysiology of Brain and Behaviour; Breuk-gevoelige plaatsen in chromosomen bij de mens; Klinische beschrijving en moleculaire definiëring van genetische syndromen; Pathofysiologie van Hersenen en GedragThis item appears in the following Collection(s)
- Academic publications [203793]
- Faculty of Medical Sciences [80320]
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