Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification

Fetal Diagnosis and Therapy

Volumn 16, Issue 4, 2001, Pages 237-240

  Theodoropoulou, Marily ^a   Barta, Csaba ^a   Szoke, Melinda ^a   Guttman, András ^d   Staub, Maria ^a   Niederland, Tamás ^c   Sólyom, János ^b   Fekete, György ^b   Sasvari Szekely, Maria ^a  

^a SEMMELWEIS UNIVERSITY   (Hungary)

^b SEMMELWEIS UNIVERSITY   (Hungary)

^c Aladar Petz County Teaching Hospital   (Hungary)

^d SYNGENTA BIOTECHNOLOGY INC   (United States)

Author keywords

Allele specific amplification; CYP21 gene; Genotyping; PCR; Prenatal diagnosis

Indexed keywords

DEXAMETHASONE; GLUCOCORTICOID; MINERALOCORTICOID;

ALLELISM; ARTICLE; CASE REPORT; CHORION VILLUS; CONGENITAL ADRENAL HYPERPLASIA; DNA DETERMINATION; FETUS; GENITAL MALFORMATION; GENOTYPE; HUMAN; NONSENSE MUTATION; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SALT LOSING NEPHRITIS; STEROID 21 MONOOXYGENASE DEFICIENCY; VIRILIZATION;

ADRENAL HYPERPLASIA, CONGENITAL; ALLELES; DEXAMETHASONE; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; GLUCOCORTICOIDS; HUMANS; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS; STEROID 21-HYDROXYLASE;

EID: 0034955985     PISSN: 10153837     EISSN: None     Source Type: Journal    
DOI: 10.1159/000053918     Document Type: Article

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