F Hecht|T W Glover|B Kaiser-Hecht - JoVE Visualize

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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.

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.

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.

Human Genetics|January 1, 1985

Human chromosome variation with two Robertsonian translocationsR Morgan, H Bixenman, F Hecht

Clinical Genetics|February 1, 1986

Congenital cutis laxa with retardation of growth and motor development: a recessive disorder of connective tissue with male lethalityJ Allanson, W Austin, F Hecht

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.

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.

Oncogene|May 30, 2006

Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sitesS G Durkin, M F Arlt, N G Howlett, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 1, 1979

Ultraviolet light induction of diphtheria toxin-resistant mutants of normal and xeroderma pigmentosum human fibroblastsT W Glover, C C Chang, J E Trosko, et al.

Pageof 22

Showing results (41-50 of 213) with videos related to

Sort By:

Pageof 22

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.

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.

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.

Human Genetics|January 1, 1985

Human chromosome variation with two Robertsonian translocationsR Morgan, H Bixenman, F Hecht

Clinical Genetics|February 1, 1986

Congenital cutis laxa with retardation of growth and motor development: a recessive disorder of connective tissue with male lethalityJ Allanson, W Austin, F Hecht

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.

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.

Oncogene|May 30, 2006

Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sitesS G Durkin, M F Arlt, N G Howlett, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 1, 1979

Ultraviolet light induction of diphtheria toxin-resistant mutants of normal and xeroderma pigmentosum human fibroblastsT W Glover, C C Chang, J E Trosko, et al.

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