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Thomas Klemm

Showing results (1-10 of 6) with videos related to

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Zeitschrift Fur Medizinische Physik|October 18, 2003
[Artifacts in MRT caused by instruments and implants]Hansjörg Graf, Ulrike A Lauer, Thomas Klemm, et al.
Parasitology Research|December 10, 2015
Highly specific detection of Cryptosporidium spp. oocysts in human stool samples by undemanding and inexpensive phase contrast microscopyRalf Ignatius, Thomas Klemm, Steffen Zander, et al.
Molecular Vision|April 28, 2012
Study of a US cohort supports the role of ZNF644 and high-grade myopia susceptibilityKhanh-Nhat Tran-Viet, Elizabeth St Germain, Vincent Soler, et al.
Ophthalmic Genetics|January 18, 2017
Reduced penetrance in a large Caucasian pedigree with Stickler syndromeStuart W Tompson, Charles Johnson, Diana Abbott, et al.
American Journal of Ophthalmology|December 11, 2012
CYP1B1, MYOC, and LTBP2 mutations in primary congenital glaucoma patients in the United StatesSing-Hui Lim, Khanh-Nhat Tran-Viet, Tammy L Yanovitch, et al.
American Journal of Human Genetics|May 7, 2013
Mutations in SCO2 are associated with autosomal-dominant high-grade myopiaKhanh-Nhat Tran-Viet, Caldwell Powell, Veluchamy A Barathi, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Zeitschrift Fur Medizinische Physik|October 18, 2003
[Artifacts in MRT caused by instruments and implants]Hansjörg Graf, Ulrike A Lauer, Thomas Klemm, et al.
Parasitology Research|December 10, 2015
Highly specific detection of Cryptosporidium spp. oocysts in human stool samples by undemanding and inexpensive phase contrast microscopyRalf Ignatius, Thomas Klemm, Steffen Zander, et al.
Molecular Vision|April 28, 2012
Study of a US cohort supports the role of ZNF644 and high-grade myopia susceptibilityKhanh-Nhat Tran-Viet, Elizabeth St Germain, Vincent Soler, et al.
Ophthalmic Genetics|January 18, 2017
Reduced penetrance in a large Caucasian pedigree with Stickler syndromeStuart W Tompson, Charles Johnson, Diana Abbott, et al.
American Journal of Ophthalmology|December 11, 2012
CYP1B1, MYOC, and LTBP2 mutations in primary congenital glaucoma patients in the United StatesSing-Hui Lim, Khanh-Nhat Tran-Viet, Tammy L Yanovitch, et al.
American Journal of Human Genetics|May 7, 2013
Mutations in SCO2 are associated with autosomal-dominant high-grade myopiaKhanh-Nhat Tran-Viet, Caldwell Powell, Veluchamy A Barathi, et al.
Pageof 1