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Somatic Cell Genetics
|
May 1, 1976
33258 Hoechst enhancement of the photosensitivity of bromodeoxyuridine-substituted cells
G 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 cases
D 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 chromosome
A 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 lines
J D Weaver, G Stetten, J W Littlefield
Human Genetics
|
January 1, 1984
Prenatal detection of an unstable ring 21 chromosome
G 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 miscarriages
G Stetten, B Sroka, M Norbury-Glaser, et al.
Prenatal Diagnosis
|
July 1, 1990
The significance of trisomy 7 mosaicism in chorionic villus cultures
K 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 syndrome
J R Wax, K J Blakemore, I Baser, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 74) with videos related to
Sort By:
Page
of 8
Somatic Cell Genetics
|
May 1, 1976
33258 Hoechst enhancement of the photosensitivity of bromodeoxyuridine-substituted cells
G 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 cases
D 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 chromosome
A 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 lines
J D Weaver, G Stetten, J W Littlefield
Human Genetics
|
January 1, 1984
Prenatal detection of an unstable ring 21 chromosome
G 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 miscarriages
G Stetten, B Sroka, M Norbury-Glaser, et al.
Prenatal Diagnosis
|
July 1, 1990
The significance of trisomy 7 mosaicism in chorionic villus cultures
K 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 syndrome
J R Wax, K J Blakemore, I Baser, et al.
Page
of 8