21-Hydroxylase deficiency in Italy: A distinct distribution pattern of CYP21 mutations in a sample from southern Italy [3]

Journal of Medical Genetics

Volumn 36, Issue 8, 1999, Pages 648-650

  Bobba, A ^a   Marra, E ^a   Giannattasio, S ^a   Iolascon, A ^a   Monno, F ^a   Di Maio, S ^a  

^a CNR   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

STEROID 21 MONOOXYGENASE;

CLINICAL ARTICLE; GENE FREQUENCY; GENE MUTATION; GENOTYPE; HUMAN; HUMAN CELL; ITALY; LETTER; PHENOTYPE; PRIORITY JOURNAL; STEROID 21 MONOOXYGENASE DEFICIENCY;

ADRENAL HYPERPLASIA, CONGENITAL; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC SCREENING; HUMANS; ITALY; MALE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; STEROID 21-HYDROXYLASE;

EID: 0032785230     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (18)