Search research articles
Contact Us
Filters
Showing results (21-30 of 42) with videos related to
Page
of 5
Sort By:
Pediatric Dermatology
|
December 4, 2004
What syndrome is this? Hunter Syndrome
Cheryl L Lonergan, Amy R Payne, William G Wilson, et al.
The Journal of Extra-Corporeal Technology
|
March 17, 2017
Veno-Venous Extracorporeal Membrane Oxygenation for Continuous Renal Replacement in a Neonate with Propionic Acidemia
Jeffrey W Gander, Erika T Rhone, William G Wilson, et al.
Molecular Genetics and Metabolism
|
July 31, 2009
Desensitization of an adult patient with Pompe disease and a history of anaphylaxis to alglucosidase alfa
Shawn E Lipinski, Michael J Lipinski, Autumn Burnette, et al.
The Journal of Biological Chemistry
|
September 26, 2003
In vitro and in vivo interactions of homocysteine with human plasma transthyretin
Amareth Lim, Shantanu Sengupta, Mark E McComb, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 20, 2020
Training the next generation of genomic medicine providers: trends in medical education and national assessment
Shoumita Dasgupta, Gerald L Feldman, Cynthia M Powell, et al.
Trends in Ecology & Evolution
|
June 30, 2006
Using ecosystem engineers to restore ecological systems
James E Byers, Kim Cuddington, Clive G Jones, et al.
Ecology Letters
|
January 30, 2007
Ecosystem engineering in space and time
Alan Hastings, James E Byers, Jeffrey A Crooks, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Hepatoblastoma and heart transplantation in a patient with cardio-facio-cutaneous syndrome
Mohamad M Al-Rahawan, Deborah J Chute, Katia Sol-Church, et al.
Journal of Medical Genetics
|
December 1, 2019
Linked-read genome sequencing identifies biallelic pathogenic variants in <i>DONSON</i> as a novel cause of Meier-Gorlin syndrome
Karen M Knapp, Rosie Sullivan, Jennie Murray, et al.
Human Genetics
|
January 18, 2022
Biochemical analysis of novel NAA10 variants suggests distinct pathogenic mechanisms involving impaired protein N-terminal acetylation
Nina McTiernan, Lisbeth Tranebjærg, Anna S Bjørheim, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 42) with videos related to
Sort By:
Page
of 5
Pediatric Dermatology
|
December 4, 2004
What syndrome is this? Hunter Syndrome
Cheryl L Lonergan, Amy R Payne, William G Wilson, et al.
The Journal of Extra-Corporeal Technology
|
March 17, 2017
Veno-Venous Extracorporeal Membrane Oxygenation for Continuous Renal Replacement in a Neonate with Propionic Acidemia
Jeffrey W Gander, Erika T Rhone, William G Wilson, et al.
Molecular Genetics and Metabolism
|
July 31, 2009
Desensitization of an adult patient with Pompe disease and a history of anaphylaxis to alglucosidase alfa
Shawn E Lipinski, Michael J Lipinski, Autumn Burnette, et al.
The Journal of Biological Chemistry
|
September 26, 2003
In vitro and in vivo interactions of homocysteine with human plasma transthyretin
Amareth Lim, Shantanu Sengupta, Mark E McComb, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 20, 2020
Training the next generation of genomic medicine providers: trends in medical education and national assessment
Shoumita Dasgupta, Gerald L Feldman, Cynthia M Powell, et al.
Trends in Ecology & Evolution
|
June 30, 2006
Using ecosystem engineers to restore ecological systems
James E Byers, Kim Cuddington, Clive G Jones, et al.
Ecology Letters
|
January 30, 2007
Ecosystem engineering in space and time
Alan Hastings, James E Byers, Jeffrey A Crooks, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Hepatoblastoma and heart transplantation in a patient with cardio-facio-cutaneous syndrome
Mohamad M Al-Rahawan, Deborah J Chute, Katia Sol-Church, et al.
Journal of Medical Genetics
|
December 1, 2019
Linked-read genome sequencing identifies biallelic pathogenic variants in <i>DONSON</i> as a novel cause of Meier-Gorlin syndrome
Karen M Knapp, Rosie Sullivan, Jennie Murray, et al.
Human Genetics
|
January 18, 2022
Biochemical analysis of novel NAA10 variants suggests distinct pathogenic mechanisms involving impaired protein N-terminal acetylation
Nina McTiernan, Lisbeth Tranebjærg, Anna S Bjørheim, et al.
Page
of 5