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K A Leppig

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Brain Research. Molecular Brain Research|October 1, 1994
Cytotoxicity mediated by conditional expression of a carboxyl-terminal derivative of the beta-amyloid precursor proteinB L Sopher, K Fukuchi, A C Smith, et al.
Teratology|December 1, 1987
Predictive value of minor anomalies: II. Use in cohort studies to identify teratogensL B Holmes, B C Kleiner, K A Leppig, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1993
Use of yeast artificial chromosomes (YACs) for studying control of gene expression: correct regulation of the genes of a human beta-globin locus YAC following transfer to mouse erythroleukemia cell linesK R Peterson, G Zitnik, C Huxley, et al.
Human Molecular Genetics|July 1, 1993
Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XISTK A Leppig, C J Brown, S L Bressler, et al.
Journal of Medical Genetics|September 6, 2005
Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1A Slavotinek, S S Lee, R Davis, et al.
Cytogenetics and Cell Genetics|January 1, 1996
The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridizationK A Leppig, D Viskochil, S Neil, et al.
Human Molecular Genetics|January 1, 1995
Deletions of both alpha 5(IV) and alpha 6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumoursL Heidet, K Dahan, J Zhou, et al.
Kidney International|December 1, 1995
Smooth muscle tumors associated with X-linked Alport syndrome: carrier detection in femalesK Dahan, L Heidet, J Zhou, et al.
Cell|January 15, 1993
DNA deletion associated with hereditary neuropathy with liability to pressure palsiesP F Chance, M K Alderson, K A Leppig, et al.
Clinical Pharmacology and Therapeutics|June 25, 2014
Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systemsL J Rasmussen-Torvik, S C Stallings, A S Gordon, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Brain Research. Molecular Brain Research|October 1, 1994
Cytotoxicity mediated by conditional expression of a carboxyl-terminal derivative of the beta-amyloid precursor proteinB L Sopher, K Fukuchi, A C Smith, et al.
Teratology|December 1, 1987
Predictive value of minor anomalies: II. Use in cohort studies to identify teratogensL B Holmes, B C Kleiner, K A Leppig, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1993
Use of yeast artificial chromosomes (YACs) for studying control of gene expression: correct regulation of the genes of a human beta-globin locus YAC following transfer to mouse erythroleukemia cell linesK R Peterson, G Zitnik, C Huxley, et al.
Human Molecular Genetics|July 1, 1993
Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XISTK A Leppig, C J Brown, S L Bressler, et al.
Journal of Medical Genetics|September 6, 2005
Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1A Slavotinek, S S Lee, R Davis, et al.
Cytogenetics and Cell Genetics|January 1, 1996
The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridizationK A Leppig, D Viskochil, S Neil, et al.
Human Molecular Genetics|January 1, 1995
Deletions of both alpha 5(IV) and alpha 6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumoursL Heidet, K Dahan, J Zhou, et al.
Kidney International|December 1, 1995
Smooth muscle tumors associated with X-linked Alport syndrome: carrier detection in femalesK Dahan, L Heidet, J Zhou, et al.
Cell|January 15, 1993
DNA deletion associated with hereditary neuropathy with liability to pressure palsiesP F Chance, M K Alderson, K A Leppig, et al.
Clinical Pharmacology and Therapeutics|June 25, 2014
Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systemsL J Rasmussen-Torvik, S C Stallings, A S Gordon, et al.
Pageof 2