SCOPUS 정보 검색 플랫폼

European Journal of Pediatrics

Volumn 145, Issue 4, 1986, Pages 260-266

Possibilities of selective screening for inborn errors of metabolism using high-resolution 1H-FT-NMR spectrometry

(2) Lehnert, W a Hunkler, D b

a UNIVERSITY OF FREIBURG (Germany)

b Chemisches Laboratorium ^* (Germany)

Author keywords

Inborn metabolic disorders; Proton NMR; Screening; spectrometry

Indexed keywords

CONGENITAL DISORDER; DIAGNOSIS; GENETIC SCREENING; HEREDITY; HUMAN; HUMAN CELL; INBORN ERROR OF METABOLISM; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE; PREVENTION; PRIORITY JOURNAL; URINE;

CHILD; HUMAN; HYDROGEN-ION CONCENTRATION; MAGNETIC RESONANCE SPECTROSCOPY; MASS SCREENING; METABOLISM, INBORN ERRORS;

EID: 0022470534 PISSN: 03406199 EISSN: 14321076 Source Type: Journal
DOI: 10.1007/BF00439397 Document Type: Article

Times cited : (89)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.