DOI:
10.1055/s-00029025
Journal of Pediatric Epilepsy
LinksClose Window
References
Van Lierde A, Menni F, Bedeschi MF. et al.
Healthcare transition in patients with rare genetic disorders with and without developmental disability: neurofibromatosis 1 and Williams-Beuren syndrome.
Am J Med Genet A 2013;
161A (07) 1666-1674
We do not assume any responsibility for the contents of the web pages of other providers.