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H Shaikh

Showing results (181-190 of 236) with videos related to

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The Indian Journal of Medical Research|July 1, 1993
Dengue in Gujarat state, India during 1988 & 1989P V Mahadev, V V Kollali, M L Rawal, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
A 781-kb deletion of 13q12.3 in a patient with Peters plus syndromeChad R Haldeman-Englert, Taiyabah Naeem, Elizabeth A Geiger, et al.
American Journal of Medical Genetics. Part A|February 13, 2013
Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams-Beuren syndromeMaria Delio, Kathleen Pope, Tao Wang, et al.
Human Genetics|June 2, 2007
High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumorEric M Jackson, Tamim H Shaikh, Sridharan Gururangan, et al.
American Journal of Medical Genetics. Part A|December 25, 2009
A de novo 8.8-Mb deletion of 21q21.1-q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21Chad R Haldeman-Englert, Kimberly A Chapman, Hillary Kruger, et al.
RSC Advances|May 6, 2022
Nanostructured N doped TiO<sub>2</sub> efficient stable catalyst for Kabachnik-Fields reaction under microwave irradiationSachin P Kunde, Kaluram G Kanade, Bhausaheb K Karale, et al.
Human Mutation|April 19, 2006
Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arraysJeffrey E Ming, Elizabeth Geiger, Alison C James, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 1994
African origin of human-specific polymorphic Alu insertionsM A Batzer, M Stoneking, M Alegria-Hartman, et al.
Retina (Philadelphia, Pa.)|November 13, 2015
LONG-TERM RESULTS OF COMBINED AB INTERNO TRABECULOTOMY (TRABECTOME) AND SMALL-GAUGE PARS PLANA VITRECTOMYBrian Toussaint, Michael R Petersen, Robert A Sisk, et al.
Human Molecular Genetics|May 15, 2015
Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain developmentPeter M Van Laarhoven, Leif R Neitzel, Anita M Quintana, et al.
Pageof 24

Showing results (181-190 of 236) with videos related to

Sort By:
Pageof 24
The Indian Journal of Medical Research|July 1, 1993
Dengue in Gujarat state, India during 1988 & 1989P V Mahadev, V V Kollali, M L Rawal, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
A 781-kb deletion of 13q12.3 in a patient with Peters plus syndromeChad R Haldeman-Englert, Taiyabah Naeem, Elizabeth A Geiger, et al.
American Journal of Medical Genetics. Part A|February 13, 2013
Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams-Beuren syndromeMaria Delio, Kathleen Pope, Tao Wang, et al.
Human Genetics|June 2, 2007
High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumorEric M Jackson, Tamim H Shaikh, Sridharan Gururangan, et al.
American Journal of Medical Genetics. Part A|December 25, 2009
A de novo 8.8-Mb deletion of 21q21.1-q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21Chad R Haldeman-Englert, Kimberly A Chapman, Hillary Kruger, et al.
RSC Advances|May 6, 2022
Nanostructured N doped TiO<sub>2</sub> efficient stable catalyst for Kabachnik-Fields reaction under microwave irradiationSachin P Kunde, Kaluram G Kanade, Bhausaheb K Karale, et al.
Human Mutation|April 19, 2006
Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arraysJeffrey E Ming, Elizabeth Geiger, Alison C James, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 1994
African origin of human-specific polymorphic Alu insertionsM A Batzer, M Stoneking, M Alegria-Hartman, et al.
Retina (Philadelphia, Pa.)|November 13, 2015
LONG-TERM RESULTS OF COMBINED AB INTERNO TRABECULOTOMY (TRABECTOME) AND SMALL-GAUGE PARS PLANA VITRECTOMYBrian Toussaint, Michael R Petersen, Robert A Sisk, et al.
Human Molecular Genetics|May 15, 2015
Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain developmentPeter M Van Laarhoven, Leif R Neitzel, Anita M Quintana, et al.
Pageof 24