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S Kenwrick

Showing results (31-40 of 57) with videos related to

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American Journal of Medical Genetics|March 10, 2001
Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infectionS Mansour, H Woffendin, S Mitton, et al.
Human Genetics|July 1, 1986
Linkage studies of X-linked recessive spastic paraplegia using DNA probesS Kenwrick, V Ionasescu, G Ionasescu, et al.
Muscle & Nerve|March 1, 1987
Molecular analysis of human muscular dystrophiesK E Davies, S Forrest, T Smith, et al.
International Journal of Cancer|August 15, 1981
Tumour cells in metastatic deposits with altered sensitivity to natural killer cellsC G Brooks, G R Flannery, N Willmott, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 1, 1981
The specificity of rat natural killer cells and cytotoxic macrophages on solid tumor-derived target cells and selected variantsC G Brooks, E A Wayner, P J Webb, et al.
Nucleic Acids Research|March 25, 1987
Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3M Patterson, S Kenwrick, S Thibodeau, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28T A Angel, C J Faust, J C Gonzales, et al.
American Journal of Human Genetics|June 1, 1995
New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndromeM Jouet, A Moncla, J Paterson, et al.
The British Journal of Ophthalmology|April 26, 2003
Novel corneal features in two males with incontinentia pigmentiE J Mayer, G N Shuttleworth, K L Greenhalgh, et al.
Genomics|September 1, 1987
Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNAJ S Waye, S J Durfy, D Pinkel, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|March 10, 2001
Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infectionS Mansour, H Woffendin, S Mitton, et al.
Human Genetics|July 1, 1986
Linkage studies of X-linked recessive spastic paraplegia using DNA probesS Kenwrick, V Ionasescu, G Ionasescu, et al.
Muscle & Nerve|March 1, 1987
Molecular analysis of human muscular dystrophiesK E Davies, S Forrest, T Smith, et al.
International Journal of Cancer|August 15, 1981
Tumour cells in metastatic deposits with altered sensitivity to natural killer cellsC G Brooks, G R Flannery, N Willmott, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 1, 1981
The specificity of rat natural killer cells and cytotoxic macrophages on solid tumor-derived target cells and selected variantsC G Brooks, E A Wayner, P J Webb, et al.
Nucleic Acids Research|March 25, 1987
Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3M Patterson, S Kenwrick, S Thibodeau, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28T A Angel, C J Faust, J C Gonzales, et al.
American Journal of Human Genetics|June 1, 1995
New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndromeM Jouet, A Moncla, J Paterson, et al.
The British Journal of Ophthalmology|April 26, 2003
Novel corneal features in two males with incontinentia pigmentiE J Mayer, G N Shuttleworth, K L Greenhalgh, et al.
Genomics|September 1, 1987
Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNAJ S Waye, S J Durfy, D Pinkel, et al.
Pageof 6