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G Stetten

Showing results (41-50 of 63) with videos related to

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Human Genetics|September 1, 1993
A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridizationD A Batista, C M Tuck-Muller, J E Martinez, et al.
American Journal of Medical Genetics|January 10, 1997
A paternally derived inverted duplication of 7q with evidence of a telomeric deletionG Stetten, L L Charity, L M Kasch, et al.
Prenatal Diagnosis|December 11, 1999
Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)patB K Goodman, K Stone, J M Coddett, et al.
American Journal of Human Genetics|April 1, 1992
Analysis of reciprocal translocations by chromosome painting: applications and limitations of the techniqueC Rosenberg, K J Blakemore, W G Kearns, et al.
American Journal of Respiratory Cell and Molecular Biology|April 1, 1991
A cystic fibrosis bronchial epithelial cell line: immortalization by adeno-12-SV40 infectionP L Zeitlin, L Lu, J Rhim, et al.
American Journal of Medical Genetics|December 1, 1990
Sexual discordance in monozygotic twinsE J Perlman, G Stetten, C M Tuck-Müller, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditismP Y Fechner, C Rosenberg, G Stetten, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panelC M Tuck-Muller, B K Goodman, S Li, et al.
Human Genetics|February 1, 1992
The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditismG D Berkovitz, P Y Fechner, S M Marcantonio, et al.
American Journal of Medical Genetics|March 17, 1997
Segregation of a familial balanced (12;10) insertion resulting in Dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in first cousinsK F Doheny, S A Rasmussen, J Rutberg, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
Human Genetics|September 1, 1993
A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridizationD A Batista, C M Tuck-Muller, J E Martinez, et al.
American Journal of Medical Genetics|January 10, 1997
A paternally derived inverted duplication of 7q with evidence of a telomeric deletionG Stetten, L L Charity, L M Kasch, et al.
Prenatal Diagnosis|December 11, 1999
Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)patB K Goodman, K Stone, J M Coddett, et al.
American Journal of Human Genetics|April 1, 1992
Analysis of reciprocal translocations by chromosome painting: applications and limitations of the techniqueC Rosenberg, K J Blakemore, W G Kearns, et al.
American Journal of Respiratory Cell and Molecular Biology|April 1, 1991
A cystic fibrosis bronchial epithelial cell line: immortalization by adeno-12-SV40 infectionP L Zeitlin, L Lu, J Rhim, et al.
American Journal of Medical Genetics|December 1, 1990
Sexual discordance in monozygotic twinsE J Perlman, G Stetten, C M Tuck-Müller, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditismP Y Fechner, C Rosenberg, G Stetten, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panelC M Tuck-Muller, B K Goodman, S Li, et al.
Human Genetics|February 1, 1992
The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditismG D Berkovitz, P Y Fechner, S M Marcantonio, et al.
American Journal of Medical Genetics|March 17, 1997
Segregation of a familial balanced (12;10) insertion resulting in Dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in first cousinsK F Doheny, S A Rasmussen, J Rutberg, et al.
Pageof 7