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W Padberg

Showing results (161-170 of 228) with videos related to

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Pediatric Neurology|August 11, 2004
Sequence analysis of the PLEXIN-D1 gene in Möbius syndrome patientsBert van der Zwaag, Harriette T F M Verzijl, Karin H Wichers, et al.
European Journal of Human Genetics : EJHG|August 17, 2006
Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genesCaroline B Michielse, Meena Bhat, Angela Brady, 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.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|November 2, 2002
PLEXIN-D1, a novel plexin family member, is expressed in vascular endothelium and the central nervous system during mouse embryogenesisBert van der Zwaag, Anita J C G M Hellemons, William P J Leenders, 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.
Langenbeck'S Archives of Surgery|February 24, 2023
Sarcopenia of kidney transplant recipients as a predictive marker for reduced graft function and graft survival after kidney transplantationH Karakizlis, N Trudel, A Brose, et al.
Journal of Medical Genetics|November 2, 1999
A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD)S M van der Maarel, G Deidda, R J Lemmers, et al.
Human Molecular Genetics|November 1, 1995
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15G van Camp, P Coucke, W Balemans, et al.
Muscle & Nerve. Supplement|January 1, 1995
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35J C van Deutekom, M H Hofker, S Romberg, et al.
Pageof 23

Showing results (161-170 of 228) with videos related to

Sort By:
Pageof 23
Pediatric Neurology|August 11, 2004
Sequence analysis of the PLEXIN-D1 gene in Möbius syndrome patientsBert van der Zwaag, Harriette T F M Verzijl, Karin H Wichers, et al.
European Journal of Human Genetics : EJHG|August 17, 2006
Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genesCaroline B Michielse, Meena Bhat, Angela Brady, 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.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|November 2, 2002
PLEXIN-D1, a novel plexin family member, is expressed in vascular endothelium and the central nervous system during mouse embryogenesisBert van der Zwaag, Anita J C G M Hellemons, William P J Leenders, 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.
Langenbeck'S Archives of Surgery|February 24, 2023
Sarcopenia of kidney transplant recipients as a predictive marker for reduced graft function and graft survival after kidney transplantationH Karakizlis, N Trudel, A Brose, et al.
Journal of Medical Genetics|November 2, 1999
A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD)S M van der Maarel, G Deidda, R J Lemmers, et al.
Human Molecular Genetics|November 1, 1995
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15G van Camp, P Coucke, W Balemans, et al.
Muscle & Nerve. Supplement|January 1, 1995
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35J C van Deutekom, M H Hofker, S Romberg, et al.
Pageof 23