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T D Bird

Showing results (111-120 of 194) with videos related to

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American Journal of Human Genetics|December 1, 1990
Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I)P F Chance, T D Bird, P O'Connell, et al.
Neurology|March 27, 2002
HLA-A2 homozygosity but not heterozygosity is associated with Alzheimer diseaseS Zareparsi, D M James, J A Kaye, et al.
Annals of Neurology|January 1, 1997
Amyloid (Abeta) deposition in chromosome 1-linked Alzheimer's disease: the Volga German familiesD M Mann, T Iwatsubo, D Nochlin, et al.
American Journal of Medical Genetics|February 21, 1997
Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2W H Raskind, M A Pericak-Vance, F Lennon, et al.
Neurology|December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disordersP F Chance, M W Lensch, H Lipe, et al.
Neurology|December 1, 1992
Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1AP F Chance, T D Bird, N Matsunami, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 13, 1999
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elementsI D'Souza, P Poorkaj, M Hong, et al.
Annals of Neurology|December 1, 1983
Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I)T D Bird, J Ott, E R Giblett, et al.
Annals of Neurology|February 1, 1992
Genetic association and linkage analysis of the apolipoprotein CII locus and familial Alzheimer's diseaseG D Schellenberg, M Boehnke, E M Wijsman, et al.
Archives of Neurology|January 29, 1999
A pedigree with a novel presenilin 1 mutation at a residue that is not conserved in presenilin 2M Yasuda, K Maeda, M Hashimoto, et al.
Pageof 20

Showing results (111-120 of 194) with videos related to

Sort By:
Pageof 20
American Journal of Human Genetics|December 1, 1990
Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I)P F Chance, T D Bird, P O'Connell, et al.
Neurology|March 27, 2002
HLA-A2 homozygosity but not heterozygosity is associated with Alzheimer diseaseS Zareparsi, D M James, J A Kaye, et al.
Annals of Neurology|January 1, 1997
Amyloid (Abeta) deposition in chromosome 1-linked Alzheimer's disease: the Volga German familiesD M Mann, T Iwatsubo, D Nochlin, et al.
American Journal of Medical Genetics|February 21, 1997
Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2W H Raskind, M A Pericak-Vance, F Lennon, et al.
Neurology|December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disordersP F Chance, M W Lensch, H Lipe, et al.
Neurology|December 1, 1992
Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1AP F Chance, T D Bird, N Matsunami, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 13, 1999
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elementsI D'Souza, P Poorkaj, M Hong, et al.
Annals of Neurology|December 1, 1983
Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I)T D Bird, J Ott, E R Giblett, et al.
Annals of Neurology|February 1, 1992
Genetic association and linkage analysis of the apolipoprotein CII locus and familial Alzheimer's diseaseG D Schellenberg, M Boehnke, E M Wijsman, et al.
Archives of Neurology|January 29, 1999
A pedigree with a novel presenilin 1 mutation at a residue that is not conserved in presenilin 2M Yasuda, K Maeda, M Hashimoto, et al.
Pageof 20