SCOPUS 정보 검색 플랫폼

Volumn 70, Issue 4, 2000, Pages 322-324

Use of TaqI digestion may lead to incorrect molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

(3) Lee, Hsien Hsiung a De Wijs, Ilse J b Sistermans, Erik A b

a Kingcar Food Industrial Co (Taiwan)

b RADBOUD UNIVERSITY MEDICAL CENTER (Netherlands)

Author keywords

Congenital adrenal hyperplasia; CYP21 gene; CYP21P pseudogene; TaqI restriction enzyme

Indexed keywords

CELL DNA; MICROSATELLITE DNA; PRIMER DNA; STEROID 21 MONOOXYGENASE; TAQ POLYMERASE;

ANALYTIC METHOD; ARTICLE; CONGENITAL ADRENAL HYPERPLASIA; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DIAGNOSTIC ERROR; DNA DETERMINATION; FEMALE; GENE AMPLIFICATION; GENE DELETION; GENETIC SCREENING; HUMAN; HUMAN CELL; MALE; MARKER GENE; PRIORITY JOURNAL; PSEUDOGENE; STEROID 21 MONOOXYGENASE DEFICIENCY;

EID: 0033799957 PISSN: 10967192 EISSN: None Source Type: Journal
DOI: 10.1006/mgme.2000.3023 Document Type: Article

Times cited : (3)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.