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S R Patil

Showing results (61-70 of 84) with videos related to

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Lancet (London, England)|January 15, 1977
Diagnostic radiation and chromosome aberrationsS R Patil, F Hecht, H A Lubs, et al.
Clinical Pediatrics|January 1, 1991
Clinical management issues in males with sex chromosomal mosaicism and discordant phenotype/sex chromosomal patternsD C Van Dyke, J W Hanson, J W Moore, et al.
Cancer Genetics and Cytogenetics|October 15, 1989
Cytogenetic abnormalities in tumors of patients with von Hippel-Lindau diseaseD K Jordan, S R Patil, J E Divelbiss, et al.
Genomics|November 26, 1998
Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palateK Yoshiura, J Machida, S Daack-Hirsch, et al.
American Journal of Medical Genetics|January 1, 1979
Pentasomy X with multiple dislocationsR F Dryer, S R Patil, H U Zellweger, et al.
Human Genetics|February 1, 1994
Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21A J Cousineau, R M Lauer, M E Pierpont, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1997
Pilot studies for proficiency testing using fluorescence in situ hybridization with chromosome-specific DNA probes: a College of American Pathologists/American College of Medical Genetics ProgramG W Dewald, A R Brothman, M G Butler, et al.
Cytogenetics and Cell Genetics|January 1, 1977
Incidence of major chromosome abnormalities in childrenS R Patil, H A Lubs, J Brown, et al.
Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. Albrecht Von Graefe'S Archive for Clinical and Experimental Ophthalmology|October 1, 1979
Retinoblastoma Y79 cell line: a study of membrane structuresA L Green, E S Meek, D W White, et al.
Prenatal Diagnosis|September 1, 1990
Trisomy 12 mosaicism in phenotypically normal fetuses following prenatal detectionH E Wyandt, T Maher, N L Fisher, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
Lancet (London, England)|January 15, 1977
Diagnostic radiation and chromosome aberrationsS R Patil, F Hecht, H A Lubs, et al.
Clinical Pediatrics|January 1, 1991
Clinical management issues in males with sex chromosomal mosaicism and discordant phenotype/sex chromosomal patternsD C Van Dyke, J W Hanson, J W Moore, et al.
Cancer Genetics and Cytogenetics|October 15, 1989
Cytogenetic abnormalities in tumors of patients with von Hippel-Lindau diseaseD K Jordan, S R Patil, J E Divelbiss, et al.
Genomics|November 26, 1998
Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palateK Yoshiura, J Machida, S Daack-Hirsch, et al.
American Journal of Medical Genetics|January 1, 1979
Pentasomy X with multiple dislocationsR F Dryer, S R Patil, H U Zellweger, et al.
Human Genetics|February 1, 1994
Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21A J Cousineau, R M Lauer, M E Pierpont, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1997
Pilot studies for proficiency testing using fluorescence in situ hybridization with chromosome-specific DNA probes: a College of American Pathologists/American College of Medical Genetics ProgramG W Dewald, A R Brothman, M G Butler, et al.
Cytogenetics and Cell Genetics|January 1, 1977
Incidence of major chromosome abnormalities in childrenS R Patil, H A Lubs, J Brown, et al.
Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. Albrecht Von Graefe'S Archive for Clinical and Experimental Ophthalmology|October 1, 1979
Retinoblastoma Y79 cell line: a study of membrane structuresA L Green, E S Meek, D W White, et al.
Prenatal Diagnosis|September 1, 1990
Trisomy 12 mosaicism in phenotypically normal fetuses following prenatal detectionH E Wyandt, T Maher, N L Fisher, et al.
Pageof 9