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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 lipoproteins
Matthias 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 disorders
Alistair 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 Kingdom
Katharina Schwarze, James Buchanan, Jilles M Fermont, et al.
Clinical Genetics
|
March 13, 2019
Delineation of dominant and recessive forms of LZTR1-associated Noonan syndrome
Alistair 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 diseases
Alistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
Page
of 8
Search research articles
Search
Showing results (71-80 of 75) with videos related to
Sort By:
Page
of 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 lipoproteins
Matthias 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 disorders
Alistair 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 Kingdom
Katharina Schwarze, James Buchanan, Jilles M Fermont, et al.
Clinical Genetics
|
March 13, 2019
Delineation of dominant and recessive forms of LZTR1-associated Noonan syndrome
Alistair 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 diseases
Alistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
Page
of 8