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T W Glover

Showing results (21-30 of 97) with videos related to

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Journal of Medical Genetics|July 1, 1993
Mild phenotypic manifestation of a 7p15.3p21.2 deletionC Wang, S Maynard, T W Glover, et al.
Nature Genetics|February 1, 1993
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesisE Legius, D A Marchuk, F S Collins, et al.
The Western Journal of Medicine|October 1, 1982
Fragile X-linked mental retardation of macro-orchidismB C Moore, T W Glover, B Kaiser-McCaw, et al.
Human Genetics|January 1, 1985
Linkage and recombination between fragile X-linked mental retardation and the factor IX geneS T Warren, T W Glover, R L Davidson, et al.
Cancer Research|December 1, 1978
Effects of harman and norharman on spontaneous and ultraviolet light-induced mutagenesis in cultured Chinese hamster cellsC C Chang, M Castellazzi, T W Glover, et al.
American Journal of Medical Genetics|December 1, 1991
Molecular and cytologic studies of Ehlers-Danlos syndrome type VIIIL G Biesecker, R P Erickson, T W Glover, et al.
Annals of Human Genetics|July 1, 1991
Polymerase chain reactions with alphoid-repeat primers in combination with Alu or LINEs primers, generate chromosome-specific DNA fragmentsR P Erickson, T W Glover, B K Hall, et al.
American Journal of Human Genetics|June 30, 2001
A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes diseaseS L Dagenais, A N Adam, J W Innis, et al.
Journal of Medical Genetics|March 1, 1989
Interstitial deletion of 2(q33q36) in a child with congenital abnormalitiesJ L Gorski, M Kiyne, W Uhlmann, et al.
Pediatric Research|February 1, 1980
Comparative study of x-ray and UV induced cytotoxicity, DNA repair, and mutagenesis in Down's syndrome and normal fibroblastsL P Yotti, T W Glover, J E Trosko, et al.
Pageof 10

Showing results (21-30 of 97) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|July 1, 1993
Mild phenotypic manifestation of a 7p15.3p21.2 deletionC Wang, S Maynard, T W Glover, et al.
Nature Genetics|February 1, 1993
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesisE Legius, D A Marchuk, F S Collins, et al.
The Western Journal of Medicine|October 1, 1982
Fragile X-linked mental retardation of macro-orchidismB C Moore, T W Glover, B Kaiser-McCaw, et al.
Human Genetics|January 1, 1985
Linkage and recombination between fragile X-linked mental retardation and the factor IX geneS T Warren, T W Glover, R L Davidson, et al.
Cancer Research|December 1, 1978
Effects of harman and norharman on spontaneous and ultraviolet light-induced mutagenesis in cultured Chinese hamster cellsC C Chang, M Castellazzi, T W Glover, et al.
American Journal of Medical Genetics|December 1, 1991
Molecular and cytologic studies of Ehlers-Danlos syndrome type VIIIL G Biesecker, R P Erickson, T W Glover, et al.
Annals of Human Genetics|July 1, 1991
Polymerase chain reactions with alphoid-repeat primers in combination with Alu or LINEs primers, generate chromosome-specific DNA fragmentsR P Erickson, T W Glover, B K Hall, et al.
American Journal of Human Genetics|June 30, 2001
A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes diseaseS L Dagenais, A N Adam, J W Innis, et al.
Journal of Medical Genetics|March 1, 1989
Interstitial deletion of 2(q33q36) in a child with congenital abnormalitiesJ L Gorski, M Kiyne, W Uhlmann, et al.
Pediatric Research|February 1, 1980
Comparative study of x-ray and UV induced cytotoxicity, DNA repair, and mutagenesis in Down's syndrome and normal fibroblastsL P Yotti, T W Glover, J E Trosko, et al.
Pageof 10