Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G W Padberg

Showing results (71-80 of 114) with videos related to

Pageof 12
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.
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.
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.
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.
International Journal of Rehabilitation Research. Internationale Zeitschrift Fur Rehabilitationsforschung. Revue Internationale De Recherches De Readaptation|October 23, 1997
Vocational perspectives and neuromuscular disordersF Andries, C W Wevers, A R Wintzen, et al.
Neurology|July 23, 2003
D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detectionR J L F Lemmers, M Osborn, T Haaf, et al.
Genomics|April 1, 1991
Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridizationC Wijmenga, G W Padberg, P Moerer, et al.
Pageof 12

Showing results (71-80 of 114) with videos related to

Sort By:
Pageof 12
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.
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.
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.
International Journal of Rehabilitation Research. Internationale Zeitschrift Fur Rehabilitationsforschung. Revue Internationale De Recherches De Readaptation|October 23, 1997
Vocational perspectives and neuromuscular disordersF Andries, C W Wevers, A R Wintzen, et al.
Neurology|July 23, 2003
D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detectionR J L F Lemmers, M Osborn, T Haaf, et al.
Genomics|April 1, 1991
Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridizationC Wijmenga, G W Padberg, P Moerer, et al.
Pageof 12