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American Journal of Medical Genetics. Part A
|
January 16, 2016
Medical foods prescribed to treat methylmalonic acidemia linked with adverse outcomes for some patients: Studies explore impact of unbalanced amino acid formulation on growth, brain development
Deborah Levenson
American Journal of Medical Genetics. Part A
|
January 16, 2016
Sweeping changes proposed for "Common rule": Update would require mandatory informed consent for use of human biospecimens in research
Deborah Levenson
American Journal of Medical Genetics. Part A
|
November 18, 2014
Higher prevalence of immune deficiency syndrome found in infants: study finds nearly twice as many newborns affected by severe combined immunodeficiency than previous research had estimated
Deborah Levenson
Bulletin of the New York Academy of Medicine
|
November 1, 1986
A diamond jubilee
D Levenson
American Journal of Medical Genetics. Part A
|
January 27, 2010
New research may help differentiate similar diagnoses
Deborah Levenson
American Journal of Medical Genetics. Part A
|
January 22, 2015
Whole-exome sequencing effective at diagnosing elusive genetic disorders: tests diagnose about 25% of patients, find a variety of mutation types
Deborah Levenson
The Pharos of Alpha Omega Alpha-Honor Medical Society. Alpha Omega Alpha
|
January 1, 1979
The search for a philosophy of medicine
S Levenson
American Journal of Medical Genetics. Part A
|
January 8, 2014
Next-generation sequencing may reduce cost and wait time for some genetic diagnoses: Experts argue that clinical evaluation remains crucial
Deborah Levenson
American Journal of Medical Genetics. Part A
|
February 19, 2015
Benefits of genomic sequencing evident in pediatric diagnoses: recent study finds testing method less costly, more effective than other medical, genetic tests
Deborah Levenson
American Journal of Medical Genetics. Part A
|
June 20, 2014
New testing guidelines for hearing loss support next-generation sequencing: testing method may help determine genetic causes of hearing loss among patients whose phenotypes are not easily distinguished clinically
Deborah Levenson
Page
of 253
Search research articles
Search
Showing results (271-280 of 2,525) with videos related to
Sort By:
Page
of 253
American Journal of Medical Genetics. Part A
|
January 16, 2016
Medical foods prescribed to treat methylmalonic acidemia linked with adverse outcomes for some patients: Studies explore impact of unbalanced amino acid formulation on growth, brain development
Deborah Levenson
American Journal of Medical Genetics. Part A
|
January 16, 2016
Sweeping changes proposed for "Common rule": Update would require mandatory informed consent for use of human biospecimens in research
Deborah Levenson
American Journal of Medical Genetics. Part A
|
November 18, 2014
Higher prevalence of immune deficiency syndrome found in infants: study finds nearly twice as many newborns affected by severe combined immunodeficiency than previous research had estimated
Deborah Levenson
Bulletin of the New York Academy of Medicine
|
November 1, 1986
A diamond jubilee
D Levenson
American Journal of Medical Genetics. Part A
|
January 27, 2010
New research may help differentiate similar diagnoses
Deborah Levenson
American Journal of Medical Genetics. Part A
|
January 22, 2015
Whole-exome sequencing effective at diagnosing elusive genetic disorders: tests diagnose about 25% of patients, find a variety of mutation types
Deborah Levenson
The Pharos of Alpha Omega Alpha-Honor Medical Society. Alpha Omega Alpha
|
January 1, 1979
The search for a philosophy of medicine
S Levenson
American Journal of Medical Genetics. Part A
|
January 8, 2014
Next-generation sequencing may reduce cost and wait time for some genetic diagnoses: Experts argue that clinical evaluation remains crucial
Deborah Levenson
American Journal of Medical Genetics. Part A
|
February 19, 2015
Benefits of genomic sequencing evident in pediatric diagnoses: recent study finds testing method less costly, more effective than other medical, genetic tests
Deborah Levenson
American Journal of Medical Genetics. Part A
|
June 20, 2014
New testing guidelines for hearing loss support next-generation sequencing: testing method may help determine genetic causes of hearing loss among patients whose phenotypes are not easily distinguished clinically
Deborah Levenson
Page
of 253