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P F Chance

Showing results (31-40 of 78) with videos related to

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Human Molecular Genetics|August 1, 2000
Unequal exchange at the Charcot-Marie-Tooth disease type 1A recombination hot-spot is not elevated above the genome average rateL L Han, M P Keller, W Navidi, et al.
Pediatric Neurology|September 1, 1996
Infantile spasms associated with proximal duplication of chromosome 15qP M Bingham, N B Spinner, L Sovinsky, et al.
Clinical Genetics|May 22, 2008
Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation--a family studyF Laccone, M C Hannibal, J Neesen, et al.
Journal of Child Neurology|October 8, 1999
Clinical nosologic and genetic aspects of Joubert and related syndromesP F Chance, L Cavalier, D Satran, et al.
Neurology|April 1, 1996
Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17qJ E Pellegrino, T R Rebbeck, M J Brown, et al.
Neurology|March 14, 2001
Evidence for genetic heterogeneity in hereditary neuralgic amyotrophyG D Watts, K C O'Briant, T E Borreson, et al.
Neurogenetics|August 3, 2005
Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizuresC L Bennett, H M Huynh, P F Chance, et al.
Nature Genetics|November 1, 1993
Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) geneB B Roa, P J Dyck, H G Marks, et al.
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.
American Journal of Medical Genetics|February 2, 1996
Developmental profile in a patient with monosomy 10q and dup(17p) associated with a peripheral neuropathyJ E Pellegrino, L Pellegrino, N B Spinner, et al.
Pageof 8

Showing results (31-40 of 78) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|August 1, 2000
Unequal exchange at the Charcot-Marie-Tooth disease type 1A recombination hot-spot is not elevated above the genome average rateL L Han, M P Keller, W Navidi, et al.
Pediatric Neurology|September 1, 1996
Infantile spasms associated with proximal duplication of chromosome 15qP M Bingham, N B Spinner, L Sovinsky, et al.
Clinical Genetics|May 22, 2008
Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation--a family studyF Laccone, M C Hannibal, J Neesen, et al.
Journal of Child Neurology|October 8, 1999
Clinical nosologic and genetic aspects of Joubert and related syndromesP F Chance, L Cavalier, D Satran, et al.
Neurology|April 1, 1996
Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17qJ E Pellegrino, T R Rebbeck, M J Brown, et al.
Neurology|March 14, 2001
Evidence for genetic heterogeneity in hereditary neuralgic amyotrophyG D Watts, K C O'Briant, T E Borreson, et al.
Neurogenetics|August 3, 2005
Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizuresC L Bennett, H M Huynh, P F Chance, et al.
Nature Genetics|November 1, 1993
Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) geneB B Roa, P J Dyck, H G Marks, et al.
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.
American Journal of Medical Genetics|February 2, 1996
Developmental profile in a patient with monosomy 10q and dup(17p) associated with a peripheral neuropathyJ E Pellegrino, L Pellegrino, N B Spinner, et al.
Pageof 8