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C C Morton

Showing results (91-100 of 185) with videos related to

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Clinical Genetics|January 1, 1986
Detection and localization of an extra HLA locus in a karyotypically normal male by chromosomal in situ hybridizationC C Morton, J A Brown, I R Kirsch, et al.
Genes, Chromosomes & Cancer|December 29, 1999
Dysregulation of HMGIC in a uterine lipoleiomyoma with a complex rearrangement including chromosomes 7, 12, and 14F Pedeutour, B J Quade, K Sornberger, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 12, 1996
Pleiotropic defects in ataxia-telangiectasia protein-deficient miceA Elson, Y Wang, C J Daugherty, et al.
Human Genetics|December 1, 1992
Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell lineJ E Reynolds, J A Fletcher, C H Lytle, et al.
American Journal of Medical Genetics|January 1, 1981
Spondylocostal dysostosis associated with anal and urogenital anomalies in a Mennonite sibshipA C Casamassima, C C Morton, W E Nance, et al.
American Journal of Human Genetics|November 1, 1989
The gene for the human mast cell high-affinity IgE receptor alpha chain: chromosomal localization to Iq21-q23 and RFLP analysisI Tepler, C C Morton, A Shimizu, et al.
Genes, Chromosomes & Cancer|October 27, 1999
Primary parauterine leiomyoma with a t(6;14)P Dal Cin, B J Quade, S Weremowicz, et al.
The Journal of Experimental Medicine|October 1, 1989
The human mannose-binding protein gene. Exon structure reveals its evolutionary relationship to a human pulmonary surfactant gene and localization to chromosome 10K Sastry, G A Herman, L Day, et al.
Obstetrics and Gynecology|June 1, 1991
Cytogenetic abnormalities in uterine leiomyomataM S Rein, A J Friedman, R L Barbieri, et al.
The American Journal of Pathology|June 1, 1997
Disseminated peritoneal leiomyomatosis. Clonality analysis by X chromosome inactivation and cytogenetics of a clinically benign smooth muscle proliferationB J Quade, C M McLachlin, V Soto-Wright, et al.
Pageof 19

Showing results (91-100 of 185) with videos related to

Sort By:
Pageof 19
Clinical Genetics|January 1, 1986
Detection and localization of an extra HLA locus in a karyotypically normal male by chromosomal in situ hybridizationC C Morton, J A Brown, I R Kirsch, et al.
Genes, Chromosomes & Cancer|December 29, 1999
Dysregulation of HMGIC in a uterine lipoleiomyoma with a complex rearrangement including chromosomes 7, 12, and 14F Pedeutour, B J Quade, K Sornberger, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 12, 1996
Pleiotropic defects in ataxia-telangiectasia protein-deficient miceA Elson, Y Wang, C J Daugherty, et al.
Human Genetics|December 1, 1992
Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell lineJ E Reynolds, J A Fletcher, C H Lytle, et al.
American Journal of Medical Genetics|January 1, 1981
Spondylocostal dysostosis associated with anal and urogenital anomalies in a Mennonite sibshipA C Casamassima, C C Morton, W E Nance, et al.
American Journal of Human Genetics|November 1, 1989
The gene for the human mast cell high-affinity IgE receptor alpha chain: chromosomal localization to Iq21-q23 and RFLP analysisI Tepler, C C Morton, A Shimizu, et al.
Genes, Chromosomes & Cancer|October 27, 1999
Primary parauterine leiomyoma with a t(6;14)P Dal Cin, B J Quade, S Weremowicz, et al.
The Journal of Experimental Medicine|October 1, 1989
The human mannose-binding protein gene. Exon structure reveals its evolutionary relationship to a human pulmonary surfactant gene and localization to chromosome 10K Sastry, G A Herman, L Day, et al.
Obstetrics and Gynecology|June 1, 1991
Cytogenetic abnormalities in uterine leiomyomataM S Rein, A J Friedman, R L Barbieri, et al.
The American Journal of Pathology|June 1, 1997
Disseminated peritoneal leiomyomatosis. Clonality analysis by X chromosome inactivation and cytogenetics of a clinically benign smooth muscle proliferationB J Quade, C M McLachlin, V Soto-Wright, et al.
Pageof 19