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Human mutation

Showing results (501-510 of 6,543) with videos related to

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Human Mutation|September 12, 2000
An association study of polymorphisms in the alpha-antichymotrypsin gene for Alzheimer disease in Han-ChineseG Meng, J Yuan, L An, et al.
Human Mutation|September 12, 2000
A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasiaA Giannotti, A Tessa, C Patrono, et al.
Human Mutation|September 12, 2000
A novel frameshift mutation, c.1870delG, in exon 12 of the CFTR geneH H Seydewitz, T Gonska, M Mall, et al.
Human Mutation|September 12, 2000
A heterozygous novel C253Y mutation in the highly conserved cysteine residues of ROM1 gene is the cause of retinitis pigmentosa in a Spanish family?C Reig, M Martinez-Gimeno, M Carballo
Human Mutation|September 12, 2000
Novel intronic polymorphisms (IVS6-73A/G and IVS21+124A/G) in the glycogen-debranching enzyme (AGL) geneA Horinishi, T Murase, M Okubo
Human Mutation|September 12, 2000
Novel single nucleotide polymorphisms (SNPs) at positions 497 (T/G) and 829 (T/C) in the human c-FOS gene and haplotype associationY Umino, H Hohjoh, K Tokunaga
Human Mutation|October 3, 2000
Diverse deletions in the growth hormone receptor gene cause growth hormone insensitivity syndromeJ M Gastier, M A Berg, P Vesterhus, et al.
Human Mutation|October 3, 2000
Oligonucleotide microarray based detection of repetitive sequence changesJ G Hacia, K Edgemon, N Fang, et al.
Human Mutation|October 3, 2000
DNA 2000: International Symposium on the State-of-the-Art in Genetic Analysis, June 1-3, 2000, Boston, U.S.AP J Bray, M H Paalman
Human Mutation|October 3, 2000
Novel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA geneT Yang, C W Lam, M W Tsang, et al.
Pageof 655

Showing results (501-510 of 6,543) with videos related to

Sort By:
Pageof 655
Human Mutation|September 12, 2000
An association study of polymorphisms in the alpha-antichymotrypsin gene for Alzheimer disease in Han-ChineseG Meng, J Yuan, L An, et al.
Human Mutation|September 12, 2000
A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasiaA Giannotti, A Tessa, C Patrono, et al.
Human Mutation|September 12, 2000
A novel frameshift mutation, c.1870delG, in exon 12 of the CFTR geneH H Seydewitz, T Gonska, M Mall, et al.
Human Mutation|September 12, 2000
A heterozygous novel C253Y mutation in the highly conserved cysteine residues of ROM1 gene is the cause of retinitis pigmentosa in a Spanish family?C Reig, M Martinez-Gimeno, M Carballo
Human Mutation|September 12, 2000
Novel intronic polymorphisms (IVS6-73A/G and IVS21+124A/G) in the glycogen-debranching enzyme (AGL) geneA Horinishi, T Murase, M Okubo
Human Mutation|September 12, 2000
Novel single nucleotide polymorphisms (SNPs) at positions 497 (T/G) and 829 (T/C) in the human c-FOS gene and haplotype associationY Umino, H Hohjoh, K Tokunaga
Human Mutation|October 3, 2000
Diverse deletions in the growth hormone receptor gene cause growth hormone insensitivity syndromeJ M Gastier, M A Berg, P Vesterhus, et al.
Human Mutation|October 3, 2000
Oligonucleotide microarray based detection of repetitive sequence changesJ G Hacia, K Edgemon, N Fang, et al.
Human Mutation|October 3, 2000
DNA 2000: International Symposium on the State-of-the-Art in Genetic Analysis, June 1-3, 2000, Boston, U.S.AP J Bray, M H Paalman
Human Mutation|October 3, 2000
Novel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA geneT Yang, C W Lam, M W Tsang, et al.
Pageof 655