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G W Padberg

Showing results (101-110 of 114) with videos related to

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Neuromuscular Disorders : NMD|April 19, 2017
Respiratory function in facioscapulohumeral muscular dystrophy 1M Wohlgemuth, C G C Horlings, E L van der Kooi, et al.
Human Molecular Genetics|July 21, 1998
Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosisR J Lemmers, S M van der Maarel, J C van Deutekom, et al.
Journal of Medical Genetics|June 19, 2002
Mutation analysis in the candidate Möbius syndrome genes PGT and GATA2 on chromosome 3 and EGR2 on chromosome 10B Van Der Zwaag, H T F M Verzijl, D Beltran-Valero De Bernabe, et al.
American Journal of Human Genetics|January 13, 2000
De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10S M van der Maarel, G Deidda, R J Lemmers, et al.
Journal of Medical Genetics|November 3, 2004
FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patientsT Rijkers, G Deidda, S van Koningsbruggen, et al.
Neuromuscular Disorders : NMD|September 29, 2006
No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophyE L van der Kooi, J C de Greef, M Wohlgemuth, et al.
Human Molecular Genetics|August 1, 1997
Germline mutations in the PTEN/MMAC1 gene in patients with Cowden diseaseM R Nelen, W C van Staveren, E A Peeters, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular DystrophyR W Tim, J R Gilbert, J M Stajich, et al.
Neurology|June 15, 2007
Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the familiesA J van der Kooi, W S Frankhuizen, P G Barth, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
Pageof 12

Showing results (101-110 of 114) with videos related to

Sort By:
Pageof 12
Neuromuscular Disorders : NMD|April 19, 2017
Respiratory function in facioscapulohumeral muscular dystrophy 1M Wohlgemuth, C G C Horlings, E L van der Kooi, et al.
Human Molecular Genetics|July 21, 1998
Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosisR J Lemmers, S M van der Maarel, J C van Deutekom, et al.
Journal of Medical Genetics|June 19, 2002
Mutation analysis in the candidate Möbius syndrome genes PGT and GATA2 on chromosome 3 and EGR2 on chromosome 10B Van Der Zwaag, H T F M Verzijl, D Beltran-Valero De Bernabe, et al.
American Journal of Human Genetics|January 13, 2000
De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10S M van der Maarel, G Deidda, R J Lemmers, et al.
Journal of Medical Genetics|November 3, 2004
FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patientsT Rijkers, G Deidda, S van Koningsbruggen, et al.
Neuromuscular Disorders : NMD|September 29, 2006
No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophyE L van der Kooi, J C de Greef, M Wohlgemuth, et al.
Human Molecular Genetics|August 1, 1997
Germline mutations in the PTEN/MMAC1 gene in patients with Cowden diseaseM R Nelen, W C van Staveren, E A Peeters, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular DystrophyR W Tim, J R Gilbert, J M Stajich, et al.
Neurology|June 15, 2007
Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the familiesA J van der Kooi, W S Frankhuizen, P G Barth, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
Pageof 12