Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature
| Autor: | Gilhuis, H.J., Ravenswaaij-Arts, C.M.A. van, Hamel, B.C.J., Gabreëls, F.J.M. |
|---|---|
| Rok vydání: | 2000 |
| Předmět: |
Breuk-gevoelige plaatsen in chromosomen bij de mens
(Fragile) breakage-prone sites in human chromosomes Clinical description and delineation of genetic syndromes Pathofysiologie van Hersenen en Gedrag Pathophysiology of Brain and Behaviour Klinische beschrijving en moleculaire definiëring van genetische syndromen |
| Zdroj: | European Journal of Paediatric Neurology, 4, pp. 39-43 European Journal of Paediatric Neurology, 4, 39-43 |
| ISSN: | 1090-3798 |
| Popis: | Item does not contain fulltext |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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