Number of items at this level: 2.
Malcolmson, J., Kleyner, R., Tegay, D., Adams, W., Ward, K., Coppinger, J., Nelson, L., Meisler, M. H., Wang, K., Robison, R., Lyon, G. J.
(November 2016)
SCN8A mutation in a child presenting with seizures and developmental delays.
Cold Spring Harb Mol Case Stud, 2 (6).
a001073.
ISSN 2373-2873
Tegay, D. H., Lane, A. H., Roohi, J., Hatchwell, E.
(March 2007)
Contiguous gene deletion involving L1CAM and AVPR2 causes X-linked hydrocephalus with nephrogenic diabetes insipidus.
American Journal of Medical Genetics Part A, 143A (6).
pp. 594-598.
ISSN 1552-4825
This list was generated on Sun Dec 8 10:55:28 2024 EST.