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P Scambler

Showing results (21-30 of 58) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1993
Report of the third international workshop on human chromosome 22 mappingB S Emanuel, K Buetow, R Nussbaum, et al.
Human Genetics|January 1, 1984
The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markersT C Gilliam, P Scambler, T Robbins, et al.
American Journal of Human Genetics|May 1, 1989
Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRPX Estivill, C McLean, V Nunes, et al.
Clinical Endocrinology|April 13, 2000
Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?A Koziell, E Charmandari, P C Hindmarsh, et al.
American Journal of Human Genetics|October 3, 1998
Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated familiesF Goodman, M L Giovannucci-Uzielli, C Hall, et al.
Enzyme|January 1, 1987
The cystic fibrosis locusR Williamson, B Wainwright, C Cooper, et al.
Human Molecular Genetics|May 16, 1998
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoformsB Klamt, A Koziell, F Poulat, et al.
Human Genetics|February 1, 1993
Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridizationC Desmaze, P Scambler, M Prieur, et al.
The American Journal of Cardiology|January 1, 1995
Transposition of the great arteries associated with deletion of chromosome 22q11S Melchionda, M C Digilio, R Mingarelli, et al.
Human Genetics|January 1, 1985
Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosisP Scambler, T Robbins, C Gilliam, et al.
Pageof 6

Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
Cytogenetics and Cell Genetics|January 1, 1993
Report of the third international workshop on human chromosome 22 mappingB S Emanuel, K Buetow, R Nussbaum, et al.
Human Genetics|January 1, 1984
The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markersT C Gilliam, P Scambler, T Robbins, et al.
American Journal of Human Genetics|May 1, 1989
Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRPX Estivill, C McLean, V Nunes, et al.
Clinical Endocrinology|April 13, 2000
Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?A Koziell, E Charmandari, P C Hindmarsh, et al.
American Journal of Human Genetics|October 3, 1998
Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated familiesF Goodman, M L Giovannucci-Uzielli, C Hall, et al.
Enzyme|January 1, 1987
The cystic fibrosis locusR Williamson, B Wainwright, C Cooper, et al.
Human Molecular Genetics|May 16, 1998
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoformsB Klamt, A Koziell, F Poulat, et al.
Human Genetics|February 1, 1993
Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridizationC Desmaze, P Scambler, M Prieur, et al.
The American Journal of Cardiology|January 1, 1995
Transposition of the great arteries associated with deletion of chromosome 22q11S Melchionda, M C Digilio, R Mingarelli, et al.
Human Genetics|January 1, 1985
Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosisP Scambler, T Robbins, C Gilliam, et al.
Pageof 6