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J R Lupski

Showing results (81-90 of 209) with videos related to

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Neurology|December 1, 1993
Uniform slowing of conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1D A Kaku, G J Parry, R Malamut, et al.
Archives of Pathology & Laboratory Medicine|November 1, 1993
DNA-based identification and epidemiologic typing of bacterial pathogensJ Versalovic, C R Woods, P R Georghiou, et al.
Annals of Neurology|January 5, 2002
Compensating for central nervous system dysmyelination: females with a proteolipid protein gene duplication and sustained clinical improvementK Inoue, H Tanaka, F Scaglia, et al.
American Journal of Medical Genetics|January 2, 1995
Unique de novo interstitial deletion of chromosome 17, del(17) (q23.2q24.3) in a female newborn with multiple congenital anomaliesM L Levin, L G Shaffer, Lewis RAp6, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Molecular mechanisms for CMT1A duplication and HNPP deletionC F Boerkoel, K Inoue, L T Reiter, et al.
American Journal of Human Genetics|April 1, 1992
Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacyL Pentao, R A Lewis, D H Ledbetter, et al.
Muscle & Nerve|January 1, 1996
Longitudinal studies of the duplication form of Charcot-Marie-Tooth polyneuropathyJ M Killian, P S Tiwari, S Jacobson, et al.
Neurology|September 1, 1993
Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy associated with a segmental duplication of chromosome 17D A Kaku, G J Parry, R Malamut, et al.
Cytogenetic and Genome Research|November 12, 2003
The donor chromosome breakpoint for a jumping translocation is associated with large low-copy repeats in 21q21.3P Stankiewicz, S W Cheung, C J Shaw, et al.
Nature Genetics|May 1, 1994
Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneousM Leppert, L Baird, K L Anderson, et al.
Pageof 21

Showing results (81-90 of 209) with videos related to

Sort By:
Pageof 21
Neurology|December 1, 1993
Uniform slowing of conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1D A Kaku, G J Parry, R Malamut, et al.
Archives of Pathology & Laboratory Medicine|November 1, 1993
DNA-based identification and epidemiologic typing of bacterial pathogensJ Versalovic, C R Woods, P R Georghiou, et al.
Annals of Neurology|January 5, 2002
Compensating for central nervous system dysmyelination: females with a proteolipid protein gene duplication and sustained clinical improvementK Inoue, H Tanaka, F Scaglia, et al.
American Journal of Medical Genetics|January 2, 1995
Unique de novo interstitial deletion of chromosome 17, del(17) (q23.2q24.3) in a female newborn with multiple congenital anomaliesM L Levin, L G Shaffer, Lewis RAp6, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Molecular mechanisms for CMT1A duplication and HNPP deletionC F Boerkoel, K Inoue, L T Reiter, et al.
American Journal of Human Genetics|April 1, 1992
Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacyL Pentao, R A Lewis, D H Ledbetter, et al.
Muscle & Nerve|January 1, 1996
Longitudinal studies of the duplication form of Charcot-Marie-Tooth polyneuropathyJ M Killian, P S Tiwari, S Jacobson, et al.
Neurology|September 1, 1993
Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy associated with a segmental duplication of chromosome 17D A Kaku, G J Parry, R Malamut, et al.
Cytogenetic and Genome Research|November 12, 2003
The donor chromosome breakpoint for a jumping translocation is associated with large low-copy repeats in 21q21.3P Stankiewicz, S W Cheung, C J Shaw, et al.
Nature Genetics|May 1, 1994
Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneousM Leppert, L Baird, K L Anderson, et al.
Pageof 21