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W Padberg

Showing results (151-160 of 228) with videos related to

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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.
Journal of Medical Genetics|September 3, 2004
Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch familyC G F de Kovel, F A Hol, J G A M Heister, et al.
Annals of Neurology|January 5, 2002
Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysisLemmers RJL, P de Kievit, M van Geel, et al.
Nature Genetics|October 2, 2002
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomereRichard J L F Lemmers, Peggy de Kievit, Lodewijk Sandkuijl, 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.
Analytical Biochemistry|July 31, 1998
Simultaneous analysis of 4- and 5-series lipoxygenase and cytochrome P450 products from different biological sources by reversed-phase high-performance liquid chromatographic techniqueL Kiss, E Bieniek, N Weissmann, et al.
American Journal of Human Genetics|May 22, 2004
Mechanism and timing of mitotic rearrangements in the subtelomeric D4Z4 repeat involved in facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Petra G M Van Overveld, Lodewijk A Sandkuijl, et al.
Archives of Otolaryngology--Head & Neck Surgery|August 26, 1998
Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472R J Ensink, K Verhoeven, H A Marres, 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.
Pageof 23

Showing results (151-160 of 228) with videos related to

Sort By:
Pageof 23
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.
Journal of Medical Genetics|September 3, 2004
Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch familyC G F de Kovel, F A Hol, J G A M Heister, et al.
Annals of Neurology|January 5, 2002
Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysisLemmers RJL, P de Kievit, M van Geel, et al.
Nature Genetics|October 2, 2002
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomereRichard J L F Lemmers, Peggy de Kievit, Lodewijk Sandkuijl, 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.
Analytical Biochemistry|July 31, 1998
Simultaneous analysis of 4- and 5-series lipoxygenase and cytochrome P450 products from different biological sources by reversed-phase high-performance liquid chromatographic techniqueL Kiss, E Bieniek, N Weissmann, et al.
American Journal of Human Genetics|May 22, 2004
Mechanism and timing of mitotic rearrangements in the subtelomeric D4Z4 repeat involved in facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Petra G M Van Overveld, Lodewijk A Sandkuijl, et al.
Archives of Otolaryngology--Head & Neck Surgery|August 26, 1998
Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472R J Ensink, K Verhoeven, H A Marres, 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.
Pageof 23