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J E Hewitt

Showing results (51-60 of 64) with videos related to

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Human Molecular Genetics|August 1, 1994
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophyJ E Hewitt, R Lyle, L N Clark, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Localization of the cell death genes CPP32 and Mch-2 to human chromosome 4qJ Nasir, J L Theilmann, V Chopra, 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.
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.
Muscle & Nerve. Supplement|April 12, 2013
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.
Neuromuscular Disorders : NMD|September 1, 1993
Molecular genetics of facioscapulohumeral muscular dystrophyC Wijmenga, R R Frants, J E Hewitt, et al.
Human Molecular Genetics|December 1, 1993
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unitJ C van Deutekom, C Wijmenga, E A van Tienhoven, et al.
Gene|August 6, 1999
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb elementJ Gabriëls, M C Beckers, H Ding, et al.
Health Physics|April 1, 1978
Ames collaborative study of cosmic ray neutrons: mid-latitude flightsJ E Hewitt, L Hughes, J W Baum, 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.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|August 1, 1994
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophyJ E Hewitt, R Lyle, L N Clark, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1997
Localization of the cell death genes CPP32 and Mch-2 to human chromosome 4qJ Nasir, J L Theilmann, V Chopra, 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.
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.
Muscle & Nerve. Supplement|April 12, 2013
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.
Neuromuscular Disorders : NMD|September 1, 1993
Molecular genetics of facioscapulohumeral muscular dystrophyC Wijmenga, R R Frants, J E Hewitt, et al.
Human Molecular Genetics|December 1, 1993
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unitJ C van Deutekom, C Wijmenga, E A van Tienhoven, et al.
Gene|August 6, 1999
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb elementJ Gabriëls, M C Beckers, H Ding, et al.
Health Physics|April 1, 1978
Ames collaborative study of cosmic ray neutrons: mid-latitude flightsJ E Hewitt, L Hughes, J W Baum, 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.
Pageof 7