M H Hofker - JoVE Visualize

Showing results (61-70 of 108) with videos related to

Pageof 11

Sort By:

Human Molecular Genetics|December 1, 1996

Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1J C van Deutekom, E Bakker, R J Lemmers, et al.

Muscle & Nerve. Supplement|January 1, 1995

Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35C Wijmenga, H G Dauwerse, G W Padberg, et al.

Hepatology (Baltimore, Md.)|July 1, 1996

Altered lipid metabolism in apolipoprotein E-deficient mice does not affect cholesterol balance across the liverF Kuipers, J M van Ree, M H Hofker, et al.

Human Molecular Genetics|October 1, 1993

Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-regionC Wijmenga, T J Wright, M J Baan, et al.

Human Genetics|September 1, 1993

The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locusC Wijmenga, S T Winokur, G W Padberg, et al.

American Journal of Human Genetics|April 1, 1987

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardationM H Hofker, A A Bergen, M I Skraastad, et al.

Lancet (London, England)|March 23, 1985

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPsE Bakker, M H Hofker, N Goor, et al.

Arteriosclerosis, Thrombosis, and Vascular Biology|March 12, 1999

Binding of beta-VLDL to heparan sulfate proteoglycans requires lipoprotein lipase, whereas ApoE only modulates binding affinityF de Beer, W L Hendriks, L C van Vark, et al.

American Journal of Human Genetics|October 1, 1988

Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal XqF P Cremers, T J van de Pol, B Wieringa, et al.

Nature Genetics|September 1, 1992

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophyC Wijmenga, J E Hewitt, L A Sandkuijl, et al.

Pageof 11

Showing results (61-70 of 108) with videos related to

Sort By:

Pageof 11

Human Molecular Genetics|December 1, 1996

Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1J C van Deutekom, E Bakker, R J Lemmers, et al.

Muscle & Nerve. Supplement|January 1, 1995

Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35C Wijmenga, H G Dauwerse, G W Padberg, et al.

Hepatology (Baltimore, Md.)|July 1, 1996

Altered lipid metabolism in apolipoprotein E-deficient mice does not affect cholesterol balance across the liverF Kuipers, J M van Ree, M H Hofker, et al.

Human Molecular Genetics|October 1, 1993

Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-regionC Wijmenga, T J Wright, M J Baan, et al.

Human Genetics|September 1, 1993

The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locusC Wijmenga, S T Winokur, G W Padberg, et al.

American Journal of Human Genetics|April 1, 1987

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardationM H Hofker, A A Bergen, M I Skraastad, et al.

Lancet (London, England)|March 23, 1985

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPsE Bakker, M H Hofker, N Goor, et al.

Arteriosclerosis, Thrombosis, and Vascular Biology|March 12, 1999

Binding of beta-VLDL to heparan sulfate proteoglycans requires lipoprotein lipase, whereas ApoE only modulates binding affinityF de Beer, W L Hendriks, L C van Vark, et al.

American Journal of Human Genetics|October 1, 1988

Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal XqF P Cremers, T J van de Pol, B Wieringa, et al.

Nature Genetics|September 1, 1992

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophyC Wijmenga, J E Hewitt, L A Sandkuijl, et al.

Pageof 11