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R J Lemmers

Showing results (1-10 of 12) with videos related to

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Gene|December 2, 1999
Cloning of the murine unconventional myosin gene Myo9b and identification of alternative splicingP K Grewal, A M Jones, M Maconochie, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1997
The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8P K Grewal, J C van Deutekom, K A Mills, et al.
Human Molecular Genetics|November 25, 2000
Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticityP G van Overveld, R J Lemmers, G Deidda, et al.
Journal of Medical Genetics|February 6, 2004
Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotypeM M O Tonini, R C M Pavanello, J Gurgel-Giannetti, et al.
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.
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.
Cytogenetics and Cell Genetics|June 1, 2000
Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35M van Geel, J C van Deutekom, A van Staalduinen, et al.
Human Molecular Genetics|May 1, 1996
Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35J C van Deutekom, R J Lemmers, P K Grewal, et al.
Neurology|October 15, 2003
Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 allelesM Wohlgemuth, R J Lemmers, 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.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Gene|December 2, 1999
Cloning of the murine unconventional myosin gene Myo9b and identification of alternative splicingP K Grewal, A M Jones, M Maconochie, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1997
The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8P K Grewal, J C van Deutekom, K A Mills, et al.
Human Molecular Genetics|November 25, 2000
Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticityP G van Overveld, R J Lemmers, G Deidda, et al.
Journal of Medical Genetics|February 6, 2004
Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotypeM M O Tonini, R C M Pavanello, J Gurgel-Giannetti, et al.
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.
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.
Cytogenetics and Cell Genetics|June 1, 2000
Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35M van Geel, J C van Deutekom, A van Staalduinen, et al.
Human Molecular Genetics|May 1, 1996
Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35J C van Deutekom, R J Lemmers, P K Grewal, et al.
Neurology|October 15, 2003
Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 allelesM Wohlgemuth, R J Lemmers, 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.
Pageof 2