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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 17, 2008
Long-term follow-up after diagnosis resulting from newborn screening: statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children
Alex R Kemper, Coleen A Boyle, Javier Aceves, et al.
The Journal of Pediatrics
|
December 24, 2018
Evidence-Based Consensus and Systematic Review on Reducing the Time to Diagnosis of Duchenne Muscular Dystrophy
Annemieke Aartsma-Rus, Madhuri Hegde, Tawfeg Ben-Omran, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 3, 2010
Carrier testing for spinal muscular atrophy
Jonathan M Gitlin, Kenneth Fischbeck, Thomas O Crawford, et al.
Molecular Genetics and Metabolism
|
June 29, 2013
Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolism
Kathryn M Camp, Michele A Lloyd-Puryear, Lynne Yao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 17, 2006
Pompe disease diagnosis and management guideline
, Priya S Kishnani, Robert D Steiner, et al.
Molecular Genetics and Metabolism
|
March 27, 2014
Phenylketonuria Scientific Review Conference: state of the science and future research needs
Kathryn M Camp, Melissa A Parisi, Phyllis B Acosta, et al.
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of 5
Search research articles
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Showing results (41-50 of 46) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 46 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 17, 2008
Long-term follow-up after diagnosis resulting from newborn screening: statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children
Alex R Kemper, Coleen A Boyle, Javier Aceves, et al.
The Journal of Pediatrics
|
December 24, 2018
Evidence-Based Consensus and Systematic Review on Reducing the Time to Diagnosis of Duchenne Muscular Dystrophy
Annemieke Aartsma-Rus, Madhuri Hegde, Tawfeg Ben-Omran, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 3, 2010
Carrier testing for spinal muscular atrophy
Jonathan M Gitlin, Kenneth Fischbeck, Thomas O Crawford, et al.
Molecular Genetics and Metabolism
|
June 29, 2013
Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolism
Kathryn M Camp, Michele A Lloyd-Puryear, Lynne Yao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 17, 2006
Pompe disease diagnosis and management guideline
, Priya S Kishnani, Robert D Steiner, et al.
Molecular Genetics and Metabolism
|
March 27, 2014
Phenylketonuria Scientific Review Conference: state of the science and future research needs
Kathryn M Camp, Melissa A Parisi, Phyllis B Acosta, et al.
Page
of 5