Combined genetic screening and traditional biochemical screening to optimize newborn screening systems

Author:

Wang Xin,Wang Yan-Yun,Hong Dong-Yang,Zhang Zhi-Lei,Li Ya-Hong,Yang Pei-Ying,Sun Yun,Jiang Tao,Xu Zheng-Feng

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference39 articles.

1. Serving the family from birth to the medical home. Newborn screening: a blueprint for the future - a call for a national agenda on state newborn screening programs;Tonniges;Pediatrics,2000

2. Newborn screening;Sahai;Crit. Rev. Clin. Lab. Sci.,2009

3. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants;Guthrie;Pediatrics,1963

4. A simple chromatographic screening test for the detection of disorders of amino acid metabolism: A technic using whole blood or urine collected on filter paper;Efron;N. Engl. J. Med.,1964

5. Newborn screening: toward a uniform screening panel and system–executive summary;Watson;Pediatrics,2006

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