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G Stetten

Showing results (21-30 of 63) with videos related to

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In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association|October 1, 1991
Origin of chromosome rearrangements in two long-lived human keratinocyte linesC Rosenberg, G Stetten, W G Kearns, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 10, 1995
TRPC1, a human homolog of a Drosophila store-operated channelP D Wes, J Chevesich, A Jeromin, et al.
Obstetrics and Gynecology|September 1, 1992
Fetal ascitic fluid: a new source of lymphocytes for rapid chromosomal analysisJ R Wax, K J Blakemore, M J Soloski, et al.
Somatic Cell and Molecular Genetics|March 1, 1995
Molecular characterization of a deleted X chromosome (Xq13.3-Xq21.31) exhibiting random X inactivationB R Migeon, G Stetten, C Tuck-Muller, et al.
The American Journal of Physiology|December 9, 1998
Isolation and characterization of the human gene encoding Ito: further diversity by alternative mRNA splicingW Kong, S Po, T Yamagishi, et al.
The New England Journal of Medicine|May 5, 1983
Prenatal diagnosis using DNA polymorphisms. Report on 95 pregnancies at risk for sickle-cell disease or beta-thalassemiaC D Boehm, S E Antonarakis, J A Phillips, et al.
Prenatal Diagnosis|February 1, 1992
Prenatal identification of small mosaic markers of different chromosomal originsG Stetten, K J Blakemore, A M Courter, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|July 1, 1975
Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescenceS A Latt, G Stetten, L A Juergens, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1975
Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemiaS A Latt, G Stetten, L A Juergens, et al.
Urology|February 1, 1996
Ambiguous genitalia in an elderly woman with a mosaic 45,X/46,X,dic(Y)(Q11.2) karyotypeY R Smith, G Stetten, L Charity, et al.
Pageof 7

Showing results (21-30 of 63) with videos related to

Sort By:
Pageof 7
In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association|October 1, 1991
Origin of chromosome rearrangements in two long-lived human keratinocyte linesC Rosenberg, G Stetten, W G Kearns, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 10, 1995
TRPC1, a human homolog of a Drosophila store-operated channelP D Wes, J Chevesich, A Jeromin, et al.
Obstetrics and Gynecology|September 1, 1992
Fetal ascitic fluid: a new source of lymphocytes for rapid chromosomal analysisJ R Wax, K J Blakemore, M J Soloski, et al.
Somatic Cell and Molecular Genetics|March 1, 1995
Molecular characterization of a deleted X chromosome (Xq13.3-Xq21.31) exhibiting random X inactivationB R Migeon, G Stetten, C Tuck-Muller, et al.
The American Journal of Physiology|December 9, 1998
Isolation and characterization of the human gene encoding Ito: further diversity by alternative mRNA splicingW Kong, S Po, T Yamagishi, et al.
The New England Journal of Medicine|May 5, 1983
Prenatal diagnosis using DNA polymorphisms. Report on 95 pregnancies at risk for sickle-cell disease or beta-thalassemiaC D Boehm, S E Antonarakis, J A Phillips, et al.
Prenatal Diagnosis|February 1, 1992
Prenatal identification of small mosaic markers of different chromosomal originsG Stetten, K J Blakemore, A M Courter, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|July 1, 1975
Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescenceS A Latt, G Stetten, L A Juergens, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1975
Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemiaS A Latt, G Stetten, L A Juergens, et al.
Urology|February 1, 1996
Ambiguous genitalia in an elderly woman with a mosaic 45,X/46,X,dic(Y)(Q11.2) karyotypeY R Smith, G Stetten, L Charity, et al.
Pageof 7