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Severe neonatal hypotonia: high prevalence of Prader-Willi syndrome, myotonic dystrophy and spinal muscular atrophy in a molecular prospective study.
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| Document type | Communication à un colloque (Conference Paper) – Abstract, Présentation orale avec comité de sélection |
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| Publication date | 2000 |
| Language | Anglais |
| Journal information | "American Journal of Human Genetics" - Vol. 67, no. 4, p. 117-117 (2000) |
| Peer reviewed | yes |
| issn | 0002-9297 |
| e-issn | 1537-6605 |
| Publisher | Univ Chicago Press (Chicago) |
| Affiliation | UCL |
| Links |
| Bibliographic reference | Van Maldergem, L. ; Hilbert, P ; Gillerot, Y.. Severe neonatal hypotonia: high prevalence of Prader-Willi syndrome, myotonic dystrophy and spinal muscular atrophy in a molecular prospective study..In: American Journal of Human Genetics, Vol. 67, no. 4, p. 117-117 (2000) |
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| Permanent URL | http://hdl.handle.net/2078.1/62210 |