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A Ciccodicola

Showing results (41-50 of 47) with videos related to

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European Journal of Human Genetics : EJHG|September 14, 1999
Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosaM G Miano, F Testa, M Strazzullo, et al.
Human Mutation|July 20, 2001
Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domainsM G Miano, F Testa, F Filippini, et al.
Genomics|December 1, 1991
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28D Schlessinger, R D Little, D Freije, et al.
Nature Genetics|May 1, 1996
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)A Meindl, K Dry, K Herrmann, et al.
Human Molecular Genetics|February 3, 2000
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal regionA Ciccodicola, M D'Esposito, T Esposito, et al.
Gene|January 30, 2002
Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegiaC Nobile, B Hinzmann, P Scannapieco, et al.
Nature|June 6, 2000
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) ConsortiumA Smahi, G Courtois, P Vabres, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
European Journal of Human Genetics : EJHG|September 14, 1999
Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosaM G Miano, F Testa, M Strazzullo, et al.
Human Mutation|July 20, 2001
Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domainsM G Miano, F Testa, F Filippini, et al.
Genomics|December 1, 1991
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28D Schlessinger, R D Little, D Freije, et al.
Nature Genetics|May 1, 1996
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)A Meindl, K Dry, K Herrmann, et al.
Human Molecular Genetics|February 3, 2000
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal regionA Ciccodicola, M D'Esposito, T Esposito, et al.
Gene|January 30, 2002
Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegiaC Nobile, B Hinzmann, P Scannapieco, et al.
Nature|June 6, 2000
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) ConsortiumA Smahi, G Courtois, P Vabres, et al.
Pageof 5