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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 5, 2016
Should states adopt newborn screening for early infantile Krabbe disease?
David P Dimmock
Pediatric Clinics of North America
|
November 30, 2016
Presentation and Diagnostic Evaluation of Mitochondrial Disease
David P Dimmock, Michael W Lawlor
Clinics in Perinatology
|
December 3, 2014
Ethical issues in DNA sequencing in the neonate
David P Dimmock, David P Bick
Human Mutation
|
June 20, 2022
Better and faster is cheaper
Erica F Sanford Kobayashi, David P Dimmock
Molecular Genetics and Metabolism
|
May 25, 2012
Recessive deoxyguanosine kinase deficiency causes juvenile onset mitochondrial myopathy
Adam H Buchaklian, Daniel Helbling, Stephanie M Ware, et al.
Pediatric Cardiology
|
September 4, 2014
Hypertrophic cardiomyopathy: a new mutation illustrates the need for family-centered care
Daniel D Lee, Regan L Veith, David P Dimmock, et al.
Pediatrics
|
May 13, 2015
SIGIRR genetic variants in premature infants with necrotizing enterocolitis
Venkatesh Sampath, Heather Menden, Daniel Helbling, et al.
Human Gene Therapy
|
August 22, 2022
Immune Responses and Immunosuppressive Strategies for Adeno-Associated Virus-Based Gene Therapy for Treatment of Central Nervous System Disorders: Current Knowledge and Approaches
Suyash Prasad, David P Dimmock, Benjamin Greenberg, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
December 22, 2020
An online compendium of treatable genetic disorders
David Bick, Sarah L Bick, David P Dimmock, et al.
Frontiers in Pediatrics
|
March 31, 2023
Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary system
Erika T Allred, Elliot A Perens, Nicole G Coufal, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 38) with videos related to
Sort By:
Page
of 4
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 5, 2016
Should states adopt newborn screening for early infantile Krabbe disease?
David P Dimmock
Pediatric Clinics of North America
|
November 30, 2016
Presentation and Diagnostic Evaluation of Mitochondrial Disease
David P Dimmock, Michael W Lawlor
Clinics in Perinatology
|
December 3, 2014
Ethical issues in DNA sequencing in the neonate
David P Dimmock, David P Bick
Human Mutation
|
June 20, 2022
Better and faster is cheaper
Erica F Sanford Kobayashi, David P Dimmock
Molecular Genetics and Metabolism
|
May 25, 2012
Recessive deoxyguanosine kinase deficiency causes juvenile onset mitochondrial myopathy
Adam H Buchaklian, Daniel Helbling, Stephanie M Ware, et al.
Pediatric Cardiology
|
September 4, 2014
Hypertrophic cardiomyopathy: a new mutation illustrates the need for family-centered care
Daniel D Lee, Regan L Veith, David P Dimmock, et al.
Pediatrics
|
May 13, 2015
SIGIRR genetic variants in premature infants with necrotizing enterocolitis
Venkatesh Sampath, Heather Menden, Daniel Helbling, et al.
Human Gene Therapy
|
August 22, 2022
Immune Responses and Immunosuppressive Strategies for Adeno-Associated Virus-Based Gene Therapy for Treatment of Central Nervous System Disorders: Current Knowledge and Approaches
Suyash Prasad, David P Dimmock, Benjamin Greenberg, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
December 22, 2020
An online compendium of treatable genetic disorders
David Bick, Sarah L Bick, David P Dimmock, et al.
Frontiers in Pediatrics
|
March 31, 2023
Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary system
Erika T Allred, Elliot A Perens, Nicole G Coufal, et al.
Page
of 4