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S G Ryan

Showing results (11-20 of 24) with videos related to

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Annals of Neurology|May 1, 1991
Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneityS G Ryan, M Wiznitzer, C Hollman, et al.
Nature Genetics|December 1, 1993
Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexiaR Shiang, S G Ryan, Y Z Zhu, et al.
Nature Genetics|September 1, 1997
Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparingS G Ryan, P F Chance, C H Zou, et al.
The Journal of Pediatrics|May 9, 2001
Medial medullary injury during adenoidectomyP B Kang, H K Phuah, R A Zimmerman, et al.
Annals of Neurology|June 1, 1992
Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysisS G Ryan, S L Sherman, J C Terry, et al.
American Journal of Medical Genetics|June 1, 1994
Deletion 5q35.3R F Stratton, N A Tedrowe, J A Tolworthy, et al.
Nature Genetics|January 13, 1998
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy familyC Charlier, N A Singh, S G Ryan, et al.
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.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Annals of Neurology|May 1, 1991
Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneityS G Ryan, M Wiznitzer, C Hollman, et al.
Nature Genetics|December 1, 1993
Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexiaR Shiang, S G Ryan, Y Z Zhu, et al.
Nature Genetics|September 1, 1997
Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparingS G Ryan, P F Chance, C H Zou, et al.
The Journal of Pediatrics|May 9, 2001
Medial medullary injury during adenoidectomyP B Kang, H K Phuah, R A Zimmerman, et al.
Annals of Neurology|June 1, 1992
Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysisS G Ryan, S L Sherman, J C Terry, et al.
American Journal of Medical Genetics|June 1, 1994
Deletion 5q35.3R F Stratton, N A Tedrowe, J A Tolworthy, et al.
Nature Genetics|January 13, 1998
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy familyC Charlier, N A Singh, S G Ryan, et al.
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.
Pageof 3