Rapid screening method for detecting mutations in the 21-hydroxylase gene

Clinical Chemistry

Volumn 43, Issue 4, 1997, Pages 557-561

  Oriola, Josep ^a   Plensa, Isabel ^a   Machuca, Isabel ^a   Pavía, Carles ^b   Rivera Fillat, Francisca ^a  

^a HOSPITAL CLÍNIC   (Spain)

^b Hospital Universitari de Sant Joan de Deu   (Spain)

Author keywords

adrenal steroid hormone; amplification created restriction site analysis; congenital adrenal hyperplasia; heritable disorder

Indexed keywords

DNA; STEROID 21 MONOOXYGENASE;

ARTICLE; CLINICAL ARTICLE; CONGENITAL ADRENAL HYPERPLASIA; CONTROLLED STUDY; DNA HYBRIDIZATION; FEMALE; GENE MUTATION; HUMAN; HUMAN CELL; LEUKOCYTE; MALE; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PSEUDOGENE; RESTRICTION MAPPING; RESTRICTION SITE; STEROID 21 MONOOXYGENASE DEFICIENCY;

EID: 0030944111     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/43.4.557     Document Type: Article

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