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U Surti

Showing results (51-60 of 89) with videos related to

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Cancer Genetics and Cytogenetics|May 1, 1993
Chromosome 7 biclonality in uterine leiomyomaY Y Ozisik, A M Meloni, M Powell, et al.
Cancer Genetics and Cytogenetics|February 1, 1995
Translocation (6;10)(p21;q22) in uterine leiomyomasY Y Ozisik, A M Meloni, O Altungoz, et al.
Cancer Genetics and Cytogenetics|July 15, 1992
Inversion (X)(p22q13) in a uterine leiomyomaY Y Ozisik, A M Meloni, U Surti, et al.
American Journal of Medical Genetics|January 11, 1996
DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi regionP A Mowery-Rushton, D J Driscoll, R D Nicholls, et al.
American Journal of Human Genetics|July 1, 1997
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28E Pegoraro, J Whitaker, P Mowery-Rushton, et al.
Cancer Genetics and Cytogenetics|May 1, 1994
Spontaneous expression of the chromosome fragile site at 10q23 in leiomyomaY Y Ozisik, A M Meloni, J F Stone, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|January 1, 1987
Immunocytochemical localization of chorionic gonadotropin, placental lactogen, and placental alkaline phosphatase in the diagnosis of complete and partial hydatidiform molesR J Brescia, R J Kurman, C S Main, et al.
American Journal of Medical Genetics|October 26, 2002
Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumorsJ Hu, E McPherson, U Surti, et al.
Cancer Genetics and Cytogenetics|May 1, 1995
Deletion of both chromosome 7 homologues in leiomyomaK L Kingsley, A M Meloni, A M Peier, et al.
American Journal of Medical Genetics|December 30, 1996
Identification of mosaicism in Prader-Willi syndrome using fluorescent in situ hybridizationP A Mowery-Rushton, J M Hanchett, W B Zipf, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
Cancer Genetics and Cytogenetics|May 1, 1993
Chromosome 7 biclonality in uterine leiomyomaY Y Ozisik, A M Meloni, M Powell, et al.
Cancer Genetics and Cytogenetics|February 1, 1995
Translocation (6;10)(p21;q22) in uterine leiomyomasY Y Ozisik, A M Meloni, O Altungoz, et al.
Cancer Genetics and Cytogenetics|July 15, 1992
Inversion (X)(p22q13) in a uterine leiomyomaY Y Ozisik, A M Meloni, U Surti, et al.
American Journal of Medical Genetics|January 11, 1996
DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi regionP A Mowery-Rushton, D J Driscoll, R D Nicholls, et al.
American Journal of Human Genetics|July 1, 1997
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28E Pegoraro, J Whitaker, P Mowery-Rushton, et al.
Cancer Genetics and Cytogenetics|May 1, 1994
Spontaneous expression of the chromosome fragile site at 10q23 in leiomyomaY Y Ozisik, A M Meloni, J F Stone, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|January 1, 1987
Immunocytochemical localization of chorionic gonadotropin, placental lactogen, and placental alkaline phosphatase in the diagnosis of complete and partial hydatidiform molesR J Brescia, R J Kurman, C S Main, et al.
American Journal of Medical Genetics|October 26, 2002
Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumorsJ Hu, E McPherson, U Surti, et al.
Cancer Genetics and Cytogenetics|May 1, 1995
Deletion of both chromosome 7 homologues in leiomyomaK L Kingsley, A M Meloni, A M Peier, et al.
American Journal of Medical Genetics|December 30, 1996
Identification of mosaicism in Prader-Willi syndrome using fluorescent in situ hybridizationP A Mowery-Rushton, J M Hanchett, W B Zipf, et al.
Pageof 9