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P E Neumann

Showing results (51-60 of 69) with videos related to

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Annals of Neurology|January 1, 1986
Thrombotic cerebral vasculopathy associated with herpes zosterD Eidelberg, A Sotrel, D S Horoupian, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 22, 1999
A novel PAX6 frameshift mutation in a kindred from Atlantic Canada with familial aniridiaS K Gupta, A Orr, D Bulman, et al.
Behavior Genetics|May 1, 1997
Mapping quantitative trait loci for open-field behavior in miceH K Gershenfeld, P E Neumann, C Mathis, et al.
Nature Genetics|April 1, 1994
Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant miceP E Neumann, W N Frankel, V A Letts, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 15, 1992
Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophyA H Beggs, P E Neumann, K Arahata, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1996
Encyclopedia of the mouse genome V. Mouse chromosome 4B A Mock, J Stoye, J Spence, et al.
Developmental Biology|February 1, 1990
Analysis of the hotfoot (ho) locus by creation of an insertional mutation in a transgenic mouseJ W Gordon, J Uehlinger, N Dayani, et al.
American Journal of Human Genetics|October 16, 1999
Mutations in NPC1 highlight a conserved NPC1-specific cysteine-rich domainW L Greer, M J Dobson, G S Girouard, et al.
Genome|September 8, 1998
FISH mapping and inter-Alu fingerprinting define the YAC contig map around the centromeric region of human chromosome 18W L Greer, M J Dobson, P E Neumann, et al.
Journal of Medical Genetics|February 26, 2000
Absence of fragile X syndrome in Nova ScotiaR G Beresford, C Tatlidil, D C Riddell, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
Annals of Neurology|January 1, 1986
Thrombotic cerebral vasculopathy associated with herpes zosterD Eidelberg, A Sotrel, D S Horoupian, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 22, 1999
A novel PAX6 frameshift mutation in a kindred from Atlantic Canada with familial aniridiaS K Gupta, A Orr, D Bulman, et al.
Behavior Genetics|May 1, 1997
Mapping quantitative trait loci for open-field behavior in miceH K Gershenfeld, P E Neumann, C Mathis, et al.
Nature Genetics|April 1, 1994
Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant miceP E Neumann, W N Frankel, V A Letts, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 15, 1992
Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophyA H Beggs, P E Neumann, K Arahata, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1996
Encyclopedia of the mouse genome V. Mouse chromosome 4B A Mock, J Stoye, J Spence, et al.
Developmental Biology|February 1, 1990
Analysis of the hotfoot (ho) locus by creation of an insertional mutation in a transgenic mouseJ W Gordon, J Uehlinger, N Dayani, et al.
American Journal of Human Genetics|October 16, 1999
Mutations in NPC1 highlight a conserved NPC1-specific cysteine-rich domainW L Greer, M J Dobson, G S Girouard, et al.
Genome|September 8, 1998
FISH mapping and inter-Alu fingerprinting define the YAC contig map around the centromeric region of human chromosome 18W L Greer, M J Dobson, P E Neumann, et al.
Journal of Medical Genetics|February 26, 2000
Absence of fragile X syndrome in Nova ScotiaR G Beresford, C Tatlidil, D C Riddell, et al.
Pageof 7