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S-M Pulst

Showing results (61-70 of 106) with videos related to

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Archives of Otolaryngology--Head & Neck Surgery|December 1, 1993
Loss of alleles in vestibular schwannomas: use of microsatellite markers on chromosome 22J Sainz, M E Baser, N K Ragge, et al.
Archives of Neurology|November 16, 2001
The SCA12 mutation as a rare cause of spinocerebellar ataxiaJ A Cholfin, M J Sobrido, S Perlman, et al.
Neurology|October 10, 2001
SCA8 repeat expansions in ataxia: a controversial associationM J Sobrido, J A Cholfin, S Perlman, et al.
Human Molecular Genetics|July 21, 1998
The mouse SCA2 gene: cDNA sequence, alternative splicing and protein expressionT Nechiporuk, D P Huynh, K Figueroa, et al.
Archives of Neurology|October 21, 1998
Oculomotor phenotypes in autosomal dominant ataxiasN Buttner, D Geschwind, J C Jen, et al.
Human Genetics|June 1, 1990
The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17S M Pulst, J M Graham, P Fain, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Down syndrome: toward a molecular definition of the phenotypeJ R Korenberg, H Kawashima, S M Pulst, et al.
Journal of Neuropathology and Experimental Neurology|September 18, 1997
Neuronal expression and intracellular localization of presenilins in normal and Alzheimer disease brainsD P Huynh, H V Vinters, D H Ho, et al.
Neurology|December 31, 1997
Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlationsD H Geschwind, S Perlman, K P Figueroa, et al.
American Journal of Medical Genetics|September 6, 1996
Phenotypic variability in monozygotic twins with neurofibromatosis 2M E Baser, N K Ragge, V M Riccardi, et al.
Pageof 11

Showing results (61-70 of 106) with videos related to

Sort By:
Pageof 11
Archives of Otolaryngology--Head & Neck Surgery|December 1, 1993
Loss of alleles in vestibular schwannomas: use of microsatellite markers on chromosome 22J Sainz, M E Baser, N K Ragge, et al.
Archives of Neurology|November 16, 2001
The SCA12 mutation as a rare cause of spinocerebellar ataxiaJ A Cholfin, M J Sobrido, S Perlman, et al.
Neurology|October 10, 2001
SCA8 repeat expansions in ataxia: a controversial associationM J Sobrido, J A Cholfin, S Perlman, et al.
Human Molecular Genetics|July 21, 1998
The mouse SCA2 gene: cDNA sequence, alternative splicing and protein expressionT Nechiporuk, D P Huynh, K Figueroa, et al.
Archives of Neurology|October 21, 1998
Oculomotor phenotypes in autosomal dominant ataxiasN Buttner, D Geschwind, J C Jen, et al.
Human Genetics|June 1, 1990
The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17S M Pulst, J M Graham, P Fain, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Down syndrome: toward a molecular definition of the phenotypeJ R Korenberg, H Kawashima, S M Pulst, et al.
Journal of Neuropathology and Experimental Neurology|September 18, 1997
Neuronal expression and intracellular localization of presenilins in normal and Alzheimer disease brainsD P Huynh, H V Vinters, D H Ho, et al.
Neurology|December 31, 1997
Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlationsD H Geschwind, S Perlman, K P Figueroa, et al.
American Journal of Medical Genetics|September 6, 1996
Phenotypic variability in monozygotic twins with neurofibromatosis 2M E Baser, N K Ragge, V M Riccardi, et al.
Pageof 11