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G Stetten

Showing results (11-20 of 74) with videos related to

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Somatic Cell Genetics|May 1, 1976
33258 Hoechst enhancement of the photosensitivity of bromodeoxyuridine-substituted cellsG Stetten, S A Latt, R L Davidson
American Journal of Medical Genetics|November 15, 1994
Molecular analysis of a complex chromosomal rearrangement and a review of familial casesD A Batista, G S Pai, G Stetten
Human Genetics|January 1, 1981
Prenatal detection of an accessory chromosome identified as an inversion duplication (15)G Stetten, B Sroka-Zaczek, V L Corson
Obstetrics and Gynecology|June 1, 1988
Fetal anomalies associated with an inversion duplication 13 chromosomeA G Rijhsinghani, R H Hruban, G Stetten
In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association|August 1, 1991
Partial trisomies in two spontaneously arising long-lived human keratinocyte linesJ D Weaver, G Stetten, J W Littlefield
Human Genetics|January 1, 1984
Prenatal detection of an unstable ring 21 chromosomeG Stetten, B Sroka, V L Corson, et al.
American Journal of Medical Genetics|November 1, 1988
Fragile site in chromosome 12 in a patient with two miscarriagesG Stetten, B Sroka, M Norbury-Glaser, et al.
Prenatal Diagnosis|July 1, 1990
The significance of trisomy 7 mosaicism in chorionic villus culturesK S Reddy, K J Blakemore, G Stetten, et al.
Prenatal Diagnosis|September 22, 1998
Region-specific FISH probes used to identify and characterize an interstitial paracentric inv(21)(q22.1q22.3)B S Torchia, C Escallon, K J Blakemore, et al.
Obstetrics and Gynecology|May 1, 1992
Isolated fetal ascites detected by sonography: an unusual presentation of Turner syndromeJ R Wax, K J Blakemore, I Baser, et al.
Pageof 8

Showing results (11-20 of 74) with videos related to

Sort By:
Pageof 8
Somatic Cell Genetics|May 1, 1976
33258 Hoechst enhancement of the photosensitivity of bromodeoxyuridine-substituted cellsG Stetten, S A Latt, R L Davidson
American Journal of Medical Genetics|November 15, 1994
Molecular analysis of a complex chromosomal rearrangement and a review of familial casesD A Batista, G S Pai, G Stetten
Human Genetics|January 1, 1981
Prenatal detection of an accessory chromosome identified as an inversion duplication (15)G Stetten, B Sroka-Zaczek, V L Corson
Obstetrics and Gynecology|June 1, 1988
Fetal anomalies associated with an inversion duplication 13 chromosomeA G Rijhsinghani, R H Hruban, G Stetten
In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association|August 1, 1991
Partial trisomies in two spontaneously arising long-lived human keratinocyte linesJ D Weaver, G Stetten, J W Littlefield
Human Genetics|January 1, 1984
Prenatal detection of an unstable ring 21 chromosomeG Stetten, B Sroka, V L Corson, et al.
American Journal of Medical Genetics|November 1, 1988
Fragile site in chromosome 12 in a patient with two miscarriagesG Stetten, B Sroka, M Norbury-Glaser, et al.
Prenatal Diagnosis|July 1, 1990
The significance of trisomy 7 mosaicism in chorionic villus culturesK S Reddy, K J Blakemore, G Stetten, et al.
Prenatal Diagnosis|September 22, 1998
Region-specific FISH probes used to identify and characterize an interstitial paracentric inv(21)(q22.1q22.3)B S Torchia, C Escallon, K J Blakemore, et al.
Obstetrics and Gynecology|May 1, 1992
Isolated fetal ascites detected by sonography: an unusual presentation of Turner syndromeJ R Wax, K J Blakemore, I Baser, et al.
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