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American Journal of Hematology
|
March 30, 2005
Molecular genetic confirmatory testing from newborn screening samples for the common African-American, Asian Indian, Southeast Asian, and Chinese beta-thalassemia mutations
Urvashi Bhardwaj, Yao-Hua Zhang, Fred Lorey, et al.
Pediatrics
|
November 18, 2005
Changes in the epidemiology of thalassemia in North America: a new minority disease
Elliott P Vichinsky, Eric A MacKlin, John S Waye, et al.
Prenatal Diagnosis
|
August 24, 2010
Ancillary benefits of prenatal maternal serum screening achieved in the California program
N Neely Kazerouni, Robert J Currier, Christina Hodgkinson, et al.
Pediatric Blood & Cancer
|
December 9, 2008
Newborn screening for hemoglobinopathies in California
Jennifer Michlitsch, Mahin Azimi, Carolyn Hoppe, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 29, 2014
Identification of galactose-1-phosphate uridyl transferase gene common mutations in dried blood spots
Maryam R Sartippour, Roya Doroudian, Gordon Frampton, et al.
Molecular Genetics and Metabolism
|
June 16, 2012
Increased incidence of profound biotinidase deficiency among Hispanic newborns in California
Tina M Cowan, Niloufar Neely Kazerouni, Nilesh Dharajiya, et al.
Disease Markers
|
February 12, 2013
WITHDRAWN: Glycan-based biomarkers for mucopolysaccharidoses
Roger Lawrence, Jillian R Brown, Fred Lorey, et al.
Molecular Genetics and Metabolism
|
August 21, 2013
Glycan-based biomarkers for mucopolysaccharidoses
Roger Lawrence, Jillian R Brown, Fred Lorey, et al.
Metabolomics : Official Journal of the Metabolomic Society
|
February 4, 2014
Precursor-to-product ratios reflect biochemical phenotype in congenital adrenal hyperplasia
Rebecca A Hicks, Jennifer K Yee, Catherine S Mao, et al.
Pediatric Hematology and Oncology
|
July 20, 2006
Prevalence of HFE mutations in California newborns
Carolyn Hoppe, Robert M Watson, Christopher M Long, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
American Journal of Hematology
|
March 30, 2005
Molecular genetic confirmatory testing from newborn screening samples for the common African-American, Asian Indian, Southeast Asian, and Chinese beta-thalassemia mutations
Urvashi Bhardwaj, Yao-Hua Zhang, Fred Lorey, et al.
Pediatrics
|
November 18, 2005
Changes in the epidemiology of thalassemia in North America: a new minority disease
Elliott P Vichinsky, Eric A MacKlin, John S Waye, et al.
Prenatal Diagnosis
|
August 24, 2010
Ancillary benefits of prenatal maternal serum screening achieved in the California program
N Neely Kazerouni, Robert J Currier, Christina Hodgkinson, et al.
Pediatric Blood & Cancer
|
December 9, 2008
Newborn screening for hemoglobinopathies in California
Jennifer Michlitsch, Mahin Azimi, Carolyn Hoppe, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 29, 2014
Identification of galactose-1-phosphate uridyl transferase gene common mutations in dried blood spots
Maryam R Sartippour, Roya Doroudian, Gordon Frampton, et al.
Molecular Genetics and Metabolism
|
June 16, 2012
Increased incidence of profound biotinidase deficiency among Hispanic newborns in California
Tina M Cowan, Niloufar Neely Kazerouni, Nilesh Dharajiya, et al.
Disease Markers
|
February 12, 2013
WITHDRAWN: Glycan-based biomarkers for mucopolysaccharidoses
Roger Lawrence, Jillian R Brown, Fred Lorey, et al.
Molecular Genetics and Metabolism
|
August 21, 2013
Glycan-based biomarkers for mucopolysaccharidoses
Roger Lawrence, Jillian R Brown, Fred Lorey, et al.
Metabolomics : Official Journal of the Metabolomic Society
|
February 4, 2014
Precursor-to-product ratios reflect biochemical phenotype in congenital adrenal hyperplasia
Rebecca A Hicks, Jennifer K Yee, Catherine S Mao, et al.
Pediatric Hematology and Oncology
|
July 20, 2006
Prevalence of HFE mutations in California newborns
Carolyn Hoppe, Robert M Watson, Christopher M Long, et al.
Page
of 5