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C K Stein

Showing results (1-10 of 20) with videos related to

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Somatic Cell and Molecular Genetics|May 5, 1999
Modified giemsa-11 staining protocol for chromosomes of human and hybrid cellsC K Stein
American Journal of Human Genetics|September 1, 1988
Chromosome breakage and recombination at fragile sitesT W Glover, C K Stein
American Journal of Human Genetics|November 1, 1987
Induction of sister chromatid exchanges at common fragile sitesT W Glover, C K Stein
Cytogenetics and Cell Genetics|January 1, 1989
A somatic cell hybrid panel to facilitate identification of DNA sequences in the vicinity of the incontinentia pigmenti locus (IP1)J L Gorski, C K Stein, T W Glover
Journal of Medical Genetics|June 1, 1997
Delineation of 14q32.3 deletion syndromeA P Ortigas, C K Stein, L L Thomson, et al.
Journal of the American Academy of Dermatology|May 1, 1989
Incontinentia pigmenti in a male infant with Klinefelter syndromeJ S Prendiville, J L Gorski, C K Stein, et al.
Obstetrics and Gynecology|May 1, 1992
Endometrial adenocarcinoma without prior hormone replacement in a diabetic patient with gonadal dysgenesisK Kratzert-Adams, M D Adelson, S Z Badawy, et al.
Clinical Genetics|November 4, 2004
Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotypeA E Shrimpton, B R Braddock, L L Thomson, et al.
Genes, Chromosomes & Cancer|January 1, 1991
Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosisT W Glover, C K Stein, E Legius, et al.
Clinical Genetics|June 1, 1996
Interstitial 6q deletion and Prader-Willi-like phenotypeC K Stein, S E Stred, L L Thomson, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Somatic Cell and Molecular Genetics|May 5, 1999
Modified giemsa-11 staining protocol for chromosomes of human and hybrid cellsC K Stein
American Journal of Human Genetics|September 1, 1988
Chromosome breakage and recombination at fragile sitesT W Glover, C K Stein
American Journal of Human Genetics|November 1, 1987
Induction of sister chromatid exchanges at common fragile sitesT W Glover, C K Stein
Cytogenetics and Cell Genetics|January 1, 1989
A somatic cell hybrid panel to facilitate identification of DNA sequences in the vicinity of the incontinentia pigmenti locus (IP1)J L Gorski, C K Stein, T W Glover
Journal of Medical Genetics|June 1, 1997
Delineation of 14q32.3 deletion syndromeA P Ortigas, C K Stein, L L Thomson, et al.
Journal of the American Academy of Dermatology|May 1, 1989
Incontinentia pigmenti in a male infant with Klinefelter syndromeJ S Prendiville, J L Gorski, C K Stein, et al.
Obstetrics and Gynecology|May 1, 1992
Endometrial adenocarcinoma without prior hormone replacement in a diabetic patient with gonadal dysgenesisK Kratzert-Adams, M D Adelson, S Z Badawy, et al.
Clinical Genetics|November 4, 2004
Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotypeA E Shrimpton, B R Braddock, L L Thomson, et al.
Genes, Chromosomes & Cancer|January 1, 1991
Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosisT W Glover, C K Stein, E Legius, et al.
Clinical Genetics|June 1, 1996
Interstitial 6q deletion and Prader-Willi-like phenotypeC K Stein, S E Stred, L L Thomson, et al.
Pageof 2