Spinal muscular atrophy combined with congenital heart disease: a report of two cases

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Title:	Spinal muscular atrophy combined with congenital heart disease: a report of two cases
Author(s):	Mulleners, W.; Ravenswaaij-Arts, C.M.A. van ; Gabreëls, F.J.M.; Hamel, B.C.J. ; Oort, A.M. van ; Sengers, R.C.A.
Publication year:	1996
Source:	Neuropediatrics, vol. 27, iss. 6, (1996), pp. 333-334
ISSN:	0174-304X
DOI:	http://dx.doi.org/10.1055/s-2007-973805
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/141003
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Subject:	(Fragile) breakage-prone sites in human chromosomes Heartfunction and circulation Pathogenesis of the hereditary neuropathies CMT1a and HNPP Breuk-gevoelige plaatsen in chromosomen bij de mens Hartfunctie en circulatie Onderzoek naar de pathogenese van de hereditaire neuropathieen CMT1a en HNPP
Organization:	Neurosurgery Human Genetics Neurology Paediatrics
Journal title:	Neuropediatrics
Volume:	vol. 27
Issue:	iss. 6
Page start:	p. 333
Page end:	p. 334
Classification:	Blood VesselsCardiovascular Abnormalities (Non MeSH)Diagnosis, Cardiovascular (Non MeSH)Diagnosis, Computer-AssistedHeartHeart DiseasesSurgery, Cardiovascular (Non MeSH)Thoracic SurgeryVascular Diseases