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ADRENOGENITALSYNDROM; 21-HYDROXYLASEMANGEL KOMBINIERT MIT 17-DESMOLASEMANGEL. KURZE MITTEILUNG = LE SYNDROME ADRENOGENITAL; DEFICIT EN 21-HYDROXYLASE ASSOCIE A UN DEFICIT EN 17-DESMOLASE. RAPPORT BREFGLEISPACH H; BERGER H; GLATZL J et al.1974; PAEDIATR. U. PAEDOL.; OESTERR.; DA. 1974; VOL. 9; NO 3; PP. 266-270; ABS. ANGL.; BIBL. 4REF.Article

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CONGENITAL ADRENAL HYPERPLASIA CAUSED BY DEFECT IN STEROID 21-HYDROXYLASE. ESTABLISHMENT OF DEFINITIVE URINARY STEROID EXCRETION PATTERN DURING FIRST WEEKS OF LIFE = HYPERPLASIE SURRENALE CONGENITALE PROVOQUEE PAR DEFAUT DE STEROIDE 21-HYDROXYLASE. ETABLISSEMENT D'UN PROFIL DEFINITIF DE L'EXCRETION URINAIRE DE STEROIDES AU COURS DE LA PREMIERE SEMAINE DE LA VIESHACKLETON CHL.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 67; NO 3; PP. 287-298; BIBL. 10 REF.Article

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DATA ON LINKAGE RELATIONS BETWEEN GLO AND 21-HYDROXYLASEKOMPF J; SIEBERT G; RITTER H et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 3; PP. 419-420; BIBL. 8 REF.Article

EARLY DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA BY MEASUREMENT OF 17-HYDROXYPROGESTERONE. = DIAGNOSTIC PRECOCE DE L'HYPERPLASIE SURRENALIENNE CONGENITALE PAR DOSAGE DE LA 17-HYDROXYPROGESTERONEYOUSSEFNEJADIAN E; DAVID R.1975; CLIN. ENDOCRINOL.; G.B.; DA. 1975; VOL. 4; NO 4; PP. 451-454; BIBL. 10 REF.Article

SOURCES OF REDUCING EQUIVALENTS FOR THE MICROSOMAL STEROID 21-HYDROXYLATION IN ISOLATED RAT ADRENAL CELLSAJAI HAKSAR; MING TE LIN; PERON FG et al.1976; ARCH. BIOCHEM. BIOPHYS.; U.S.A.; DA. 1976; VOL. 173; NO 1; PP. 121-124; BIBL. 17 REF.Article

ETUDE DE LA 21-HYDROXYLASE DES GLANDES SURRENALES DU CANARD DOMESTIQUE (ANAS PLATYRHYNCHOS)LEBLANC H; LEHOUX JG; SANDOR T et al.1972; J. STEROID BIOCHEM.; G.B.; DA. 1972; VOL. 3; NO 4; PP. 683-692; ABS. ANGL.; BIBL. 24REF.Article

THE NATURE OF THE CYTOSOLIC ACTIVATORS OF THE ADRENAL STEROID 21-HYDROXYLATION SYSTEMPONTICORVO L; GREENFIELD N; WOLFSON A et al.1980; ARCH. BIOCHEM. BIOPHYS.; USA; DA. 1980; VOL. 200; NO 1; PP. 223-231; BIBL. 12 REF.Article

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THE EARLY RECOGNITION OF THE 21-HYDROXYLASE DEFICIENCY VARIETY OF CONGENITAL ADRENAL HYPERPLASIASTEEN G; TAS AC; TEN NOEVER DE BRAUW MC et al.1980; CLIN. CHIM. ACTA; NLD; DA. 1980; VOL. 105; NO 2; PP. 213-224; BIBL. 24 REF.Article

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SPIRONOLACTONE AND CYTOCHROME P-450: IMPAIRMENT OF STEROID 21-HYDROXYLATION IN THE ADRENAL CORTEXMENARD RH; BARTTER FC; GILLETTE JR et al.1976; ARCH. BIOCHEM. BIOPHYS.; U.S.A.; DA. 1976; VOL. 173; NO 2; PP. 395-402; BIBL. 9 REF.Article

EVIDENCE FOR PARTIAL 21-HYDROXYLASE DEFICIENCY AMONG HETEROZYGOTE CARRIERS OF CONGENITAL ADRENAL HYPERPLASIA. = PREUVE D'UNE INSUFFISANCE PARTIELLE EN 21-HYDROXYLASE PARMI LES TRANSPORTEURS HETEROZYGOTES DE L'HYPERPLASIE SURRENALIENNE CONGENITALELEE PA; GAREIS FJ.1975; J. CLIN. ENDOCRINOL. METABOL.; U.S.A.; DA. 1975; VOL. 41; NO 2; PP. 415-418; BIBL. 7 REF.Article

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