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Severe neonatal hypotonia: high prevalence of Prader-Willi syndrome, myotonic dystrophy and spinal muscular atrophy in a molecular prospective study.

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)
Permanent URL http://hdl.handle.net/2078.1/62210