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American Journal of Human Genetics|April 29, 1998
Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34P F Chance, B A Rabin, S G Ryan, et al.Cancer|August 15, 1988
Late recurrence of primitive neuroectodermal tumor/medulloblastomaI B Lefkowitz, R J Packer, S G Ryan, et al.Annals of Neurology|July 1, 1995
Mutational analysis of familial and sporadic hyperekplexiaR Shiang, S G Ryan, Y Z Zhu, et al.American Journal of Human Genetics|December 1, 1992
Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5qS G Ryan, M J Dixon, M A Nigro, et al.Nature Genetics|June 1, 1994
A missense mutation in the gene encoding the alpha 1 subunit of the inhibitory glycine receptor in the spasmodic mouseS G Ryan, M S Buckwalter, J W Lynch, et al.American Journal of Medical Genetics|July 25, 1997
Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiencyC T Gay, L J Hardies, R A Rauch, et al.Epilepsia|June 26, 2001
Lack of association between an interleukin 1 beta (IL-1beta) gene variation and refractory temporal lobe epilepsyR J Buono, T N Ferraro, M J O'Connor, et al.Epilepsy Research|May 4, 2004
Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibilityR J Buono, F W Lohoff, T Sander, et al.Pageof 4