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Trilochan Sahoo

Showing results (1-10 of 65) with videos related to

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Applied Optics|July 21, 2015
Simulation of optically encoded multiplexing for parallel multipoint sensingC Babu Rao, Pandian Chelliah, Trilochan Sahoo
Frontiers in Oncology|September 19, 2025
Case Report: Unraveling complex genomic alterations in a case of chronic lymphocytic leukemia using optical genome mappingLeila Youssefian, Trilochan Sahoo, Jia-Chi Wang
Applied Optics|November 13, 2015
Simulation of path delay multiplexing-based Fourier transform spectrometer for fiber Bragg grating interrogationPandian Chelliah, Trilochan Sahoo, Sheela Singh, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Atypical cases of Angelman syndromeAmy Lawson-Yuen, Bai-Lin Wu, Va Lip, et al.
BMC Medical Genetics|February 14, 2006
Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2)Seema R Lalani, Trilochan Sahoo, Merideth E Sanders, et al.
American Journal of Medical Genetics. Part A|June 24, 2004
Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)]Svetlana A Yatsenko, Trilochan Sahoo, Melinda Rosenkranz, et al.
American Journal of Medical Genetics. Part A|January 8, 2005
A patient with isochromosome 18q, radial-thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocationTrilochan Sahoo, Rizwan Naeem, Kim Pham, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 8, 2014
Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive casesJia-Chi Wang, Trilochan Sahoo, Steven Schonberg, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 21, 2009
The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlationsRobin P Goin-Kochel, Anne E Porter, Sarika U Peters, et al.
American Journal of Medical Genetics. Part A|November 9, 2011
Microdeletion of Xq28 involving the AFF2 (FMR2) gene in two unrelated males with developmental delayTrilochan Sahoo, Aaron Theisen, Michael Marble, et al.
Pageof 7

Showing results (1-10 of 65) with videos related to

Sort By:
Pageof 7
Applied Optics|July 21, 2015
Simulation of optically encoded multiplexing for parallel multipoint sensingC Babu Rao, Pandian Chelliah, Trilochan Sahoo
Frontiers in Oncology|September 19, 2025
Case Report: Unraveling complex genomic alterations in a case of chronic lymphocytic leukemia using optical genome mappingLeila Youssefian, Trilochan Sahoo, Jia-Chi Wang
Applied Optics|November 13, 2015
Simulation of path delay multiplexing-based Fourier transform spectrometer for fiber Bragg grating interrogationPandian Chelliah, Trilochan Sahoo, Sheela Singh, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Atypical cases of Angelman syndromeAmy Lawson-Yuen, Bai-Lin Wu, Va Lip, et al.
BMC Medical Genetics|February 14, 2006
Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2)Seema R Lalani, Trilochan Sahoo, Merideth E Sanders, et al.
American Journal of Medical Genetics. Part A|June 24, 2004
Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)]Svetlana A Yatsenko, Trilochan Sahoo, Melinda Rosenkranz, et al.
American Journal of Medical Genetics. Part A|January 8, 2005
A patient with isochromosome 18q, radial-thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocationTrilochan Sahoo, Rizwan Naeem, Kim Pham, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 8, 2014
Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive casesJia-Chi Wang, Trilochan Sahoo, Steven Schonberg, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 21, 2009
The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlationsRobin P Goin-Kochel, Anne E Porter, Sarika U Peters, et al.
American Journal of Medical Genetics. Part A|November 9, 2011
Microdeletion of Xq28 involving the AFF2 (FMR2) gene in two unrelated males with developmental delayTrilochan Sahoo, Aaron Theisen, Michael Marble, et al.
Pageof 7