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H Backhovens

Showing results (11-20 of 42) with videos related to

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Neuroscience Letters|March 14, 1994
APOE genotype does not modulate age of onset in families with chromosome 14 encoded Alzheimer's diseaseC Van Broeckhoven, H Backhovens, M Cruts, et al.
Nature Genetics|December 1, 1992
Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3C Van Broeckhoven, H Backhovens, M Cruts, et al.
The Journal of Pathology|January 1, 1997
WT1 mutation in malignant mesothelioma and WT1 immunoreactivity in relation to p53 and growth factor receptor expression, cell-type transition, and prognosisS Kumar-Singh, K Segers, U Rodeck, et al.
Human Genetics|June 1, 1991
Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniquesW Van Hul, H Backhovens, G Van Camp, et al.
Human Genetics|October 1, 1991
Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndromeG Van Camp, H Backhovens, M Cruts, et al.
Virchows Archiv : an International Journal of Pathology|January 1, 1995
Immunoreactivity for p53 and mdm2 and the detection of p53 mutations in human malignant mesotheliomaK Segers, H Backhovens, S K Singh, et al.
Human Genetics|January 1, 1988
The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1P Raeymaekers, C Van Broeckhoven, H Backhovens, et al.
Somatic Cell and Molecular Genetics|May 1, 1990
Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybridsG Van Camp, W Van Hul, H Backhovens, et al.
Human Mutation|January 1, 1997
Mutation analysis of the connexin 32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: identification of five new mutationsE Nelis, S Simokovic, V Timmerman, et al.
American Journal of Human Genetics|October 1, 1994
A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21C M van Duijn, L Hendriks, L A Farrer, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Neuroscience Letters|March 14, 1994
APOE genotype does not modulate age of onset in families with chromosome 14 encoded Alzheimer's diseaseC Van Broeckhoven, H Backhovens, M Cruts, et al.
Nature Genetics|December 1, 1992
Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3C Van Broeckhoven, H Backhovens, M Cruts, et al.
The Journal of Pathology|January 1, 1997
WT1 mutation in malignant mesothelioma and WT1 immunoreactivity in relation to p53 and growth factor receptor expression, cell-type transition, and prognosisS Kumar-Singh, K Segers, U Rodeck, et al.
Human Genetics|June 1, 1991
Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniquesW Van Hul, H Backhovens, G Van Camp, et al.
Human Genetics|October 1, 1991
Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndromeG Van Camp, H Backhovens, M Cruts, et al.
Virchows Archiv : an International Journal of Pathology|January 1, 1995
Immunoreactivity for p53 and mdm2 and the detection of p53 mutations in human malignant mesotheliomaK Segers, H Backhovens, S K Singh, et al.
Human Genetics|January 1, 1988
The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1P Raeymaekers, C Van Broeckhoven, H Backhovens, et al.
Somatic Cell and Molecular Genetics|May 1, 1990
Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybridsG Van Camp, W Van Hul, H Backhovens, et al.
Human Mutation|January 1, 1997
Mutation analysis of the connexin 32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: identification of five new mutationsE Nelis, S Simokovic, V Timmerman, et al.
American Journal of Human Genetics|October 1, 1994
A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21C M van Duijn, L Hendriks, L A Farrer, et al.
Pageof 5