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John M Taylor

Showing results (71-80 of 75) with videos related to

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Journal of Lipid Research|January 18, 2005
High-level lipoprotein [a] expression in transgenic mice: evidence for oxidized phospholipids in lipoprotein [a] but not in low density lipoproteinsMatthias Schneider, Joseph L Witztum, Stephen G Young, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disordersAlistair T Pagnamenta, Yoshiko Murakami, John M Taylor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2019
The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United KingdomKatharina Schwarze, James Buchanan, Jilles M Fermont, et al.
Clinical Genetics|March 13, 2019
Delineation of dominant and recessive forms of LZTR1-associated Noonan syndromeAlistair T Pagnamenta, Pamela J Kaisaki, Fenella Bennett, et al.
Genome Medicine|November 10, 2023
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseasesAlistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
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Showing results (71-80 of 75) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 75 results.
Journal of Lipid Research|January 18, 2005
High-level lipoprotein [a] expression in transgenic mice: evidence for oxidized phospholipids in lipoprotein [a] but not in low density lipoproteinsMatthias Schneider, Joseph L Witztum, Stephen G Young, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disordersAlistair T Pagnamenta, Yoshiko Murakami, John M Taylor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2019
The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United KingdomKatharina Schwarze, James Buchanan, Jilles M Fermont, et al.
Clinical Genetics|March 13, 2019
Delineation of dominant and recessive forms of LZTR1-associated Noonan syndromeAlistair T Pagnamenta, Pamela J Kaisaki, Fenella Bennett, et al.
Genome Medicine|November 10, 2023
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseasesAlistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
Pageof 8