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Clinical Chemistry
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July 28, 2010
A multiplex immunoassay using the Guthrie specimen to detect T-cell deficiencies including severe combined immunodeficiency disease
David K Janik, Barbara Lindau-Shepard, Anne Marie Comeau, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2008
Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: under-representation of the common c.985 A > G mutation in the New York state population
Matthew J Nichols, Carlos A Saavedra-Matiz, Kenneth A Pass, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 23, 2008
Perinatal transfer of genetic information: developing an algorithm for reporting cystic fibrosis prenatal test results to the newborn screening program
Ellen S Regalado, Elinor Langfelder-Schwind, Andrew D Corwin, et al.
Clinical Chemistry
|
May 17, 2011
Improved immunoassay for the detection of severe combined immunodeficiency
David K Janik, Barbara Lindau-Shepard, Bent Nørgaard-Pedersen, et al.
Clinical Chemistry
|
August 26, 2011
Newborn screening for metabolic disorders: how are we doing, and where are we going?
Michael J Bennett, Piero Rinaldo, Bridget Wilcken, et al.
Clinical Chemistry
|
May 26, 2005
Evaluation of glucose-6-phosphate dehydrogenase stability in blood samples under different collection and storage conditions
Simone M Castro, Raquel Weber, Vivian Dadalt, et al.
Environmental Science & Technology
|
August 30, 2008
Use of newborn screening program blood spots for exposure assessment: declining levels of perluorinated compounds in New York State infants
Henry M Spliethoff, Lin Tao, Shannon M Shaver, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 24, 2002
Characterization of beta-globin haplotypes using blood spots from a population-based cohort of newborns with homozygous HbS
Dana C Crawford, Michele Caggana, Katharine B Harris, et al.
Pediatrics
|
May 4, 2010
Trends in incidence rates of congenital hypothyroidism related to select demographic factors: data from the United States, California, Massachusetts, New York, and Texas
Cynthia F Hinton, Katharine B Harris, Lynette Borgfeld, et al.
Clinical Chemistry
|
July 28, 2010
High-throughput multiplexed T-cell-receptor excision circle quantitative PCR assay with internal controls for detection of severe combined immunodeficiency in population-based newborn screening
Jacalyn L Gerstel-Thompson, Jonathan F Wilkey, Jennifer C Baptiste, et al.
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Search research articles
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Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Clinical Chemistry
|
July 28, 2010
A multiplex immunoassay using the Guthrie specimen to detect T-cell deficiencies including severe combined immunodeficiency disease
David K Janik, Barbara Lindau-Shepard, Anne Marie Comeau, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2008
Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: under-representation of the common c.985 A > G mutation in the New York state population
Matthew J Nichols, Carlos A Saavedra-Matiz, Kenneth A Pass, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 23, 2008
Perinatal transfer of genetic information: developing an algorithm for reporting cystic fibrosis prenatal test results to the newborn screening program
Ellen S Regalado, Elinor Langfelder-Schwind, Andrew D Corwin, et al.
Clinical Chemistry
|
May 17, 2011
Improved immunoassay for the detection of severe combined immunodeficiency
David K Janik, Barbara Lindau-Shepard, Bent Nørgaard-Pedersen, et al.
Clinical Chemistry
|
August 26, 2011
Newborn screening for metabolic disorders: how are we doing, and where are we going?
Michael J Bennett, Piero Rinaldo, Bridget Wilcken, et al.
Clinical Chemistry
|
May 26, 2005
Evaluation of glucose-6-phosphate dehydrogenase stability in blood samples under different collection and storage conditions
Simone M Castro, Raquel Weber, Vivian Dadalt, et al.
Environmental Science & Technology
|
August 30, 2008
Use of newborn screening program blood spots for exposure assessment: declining levels of perluorinated compounds in New York State infants
Henry M Spliethoff, Lin Tao, Shannon M Shaver, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 24, 2002
Characterization of beta-globin haplotypes using blood spots from a population-based cohort of newborns with homozygous HbS
Dana C Crawford, Michele Caggana, Katharine B Harris, et al.
Pediatrics
|
May 4, 2010
Trends in incidence rates of congenital hypothyroidism related to select demographic factors: data from the United States, California, Massachusetts, New York, and Texas
Cynthia F Hinton, Katharine B Harris, Lynette Borgfeld, et al.
Clinical Chemistry
|
July 28, 2010
High-throughput multiplexed T-cell-receptor excision circle quantitative PCR assay with internal controls for detection of severe combined immunodeficiency in population-based newborn screening
Jacalyn L Gerstel-Thompson, Jonathan F Wilkey, Jennifer C Baptiste, et al.
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of 3