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K Holman

Showing results (31-40 of 45) with videos related to

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American Journal of Medical Genetics|July 15, 1994
Haplotype analysis at the FRAXA locus in the Japanese populationR I Richards, I Kondo, K Holman, et al.
Journal of Medical Genetics|December 1, 1991
Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile siteR I Richards, K Holman, H Kozman, et al.
Nature Genetics|July 1, 1992
Evidence of founder chromosomes in fragile X syndromeR I Richards, K Holman, K Friend, et al.
Nature|August 31, 1995
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 geneE I Rogaev, R Sherrington, E A Rogaeva, et al.
Science (New York, N.Y.)|May 24, 1991
Fragile X genotype characterized by an unstable region of DNAS Yu, M Pritchard, E Kremer, et al.
American Journal of Human Genetics|August 1, 1993
Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studiesI Aksentijevich, E Pras, L Gruberg, et al.
American Journal of Human Genetics|September 1, 1993
Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysisI Aksentijevich, E Pras, L Gruberg, et al.
Genomics|July 1, 1994
A PCR-based genetic linkage map of human chromosome 16Y Shen, H M Kozman, A Thompson, et al.
Science (New York, N.Y.)|June 24, 1994
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesisJ K Nancarrow, E Kremer, K Holman, et al.
Science (New York, N.Y.)|June 21, 1991
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)nE J Kremer, M Pritchard, M Lynch, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|July 15, 1994
Haplotype analysis at the FRAXA locus in the Japanese populationR I Richards, I Kondo, K Holman, et al.
Journal of Medical Genetics|December 1, 1991
Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile siteR I Richards, K Holman, H Kozman, et al.
Nature Genetics|July 1, 1992
Evidence of founder chromosomes in fragile X syndromeR I Richards, K Holman, K Friend, et al.
Nature|August 31, 1995
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 geneE I Rogaev, R Sherrington, E A Rogaeva, et al.
Science (New York, N.Y.)|May 24, 1991
Fragile X genotype characterized by an unstable region of DNAS Yu, M Pritchard, E Kremer, et al.
American Journal of Human Genetics|August 1, 1993
Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studiesI Aksentijevich, E Pras, L Gruberg, et al.
American Journal of Human Genetics|September 1, 1993
Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysisI Aksentijevich, E Pras, L Gruberg, et al.
Genomics|July 1, 1994
A PCR-based genetic linkage map of human chromosome 16Y Shen, H M Kozman, A Thompson, et al.
Science (New York, N.Y.)|June 24, 1994
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesisJ K Nancarrow, E Kremer, K Holman, et al.
Science (New York, N.Y.)|June 21, 1991
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)nE J Kremer, M Pritchard, M Lynch, et al.
Pageof 5