TRUE PROSTATIC TISSUE IN 46, XX FEMALE WITH ADRENOGENITAL SYNDROMEKIVIAT MD; LEONARD JM.1978; UROLOGY; USA; DA. 1978; VOL. 12; NO 1; PP. 75-78; BIBL. 25 REF.Article

INFERTILITY IN AN XX MALE.PAIS VM; VASUDEVAN P.1977; J. UROL.; U.S.A.; DA. 1977; VOL. 118; NO 4; PP. 690-691; BIBL. 10 REF.; RESUMEArticle

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Y-CHROMOSOMAL GENES IN A PHENOTYPIC MALE WITH A 46XX KARYOTYPE.DOSIK H; WACHTEL SS; FARIDA KHAN et al.1976; J.A.M.A.; U.S.A.; DA. 1976; VOL. 236; NO 22; PP. 2505-2508; BIBL. 11 REF.Article

AZOOSPERMIE CRYPTO-Y-GONOSOMIQUE. (HOMME, 46XX)PARAMO PG; IZQUIERDO L; ESCUDERO M et al.1976; ACTA UROL. BELG.; BELG.; DA. 1976; VOL. 44; NO 1; PP. 82-91; ABS. ANGL.; BIBL. 18 REF.Article

BRIQUET SYNDROME IN A MAN WITH CHRONIC INTRACTABLE PAINDE FIGUEIREDO JM; BAIARDI JJ; LONG DM et al.1980; JOHNS HOPKINS MED. J.; ISSN 0021-7263; USA; DA. 1980; VOL. 147; NO 3; PP. 102-106; BIBL. 15 REF.Article

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CYTOGENETIC STUDIES IN PRIMARY INFERTILITY.MOHAN RAO M; DORA MOHAN RAO.1977; FERTIL. AND STERIL.; U.S.A.; DA. 1977; VOL. 28; NO 2; PP. 209-210; BIBL. 5 REF.Article

THE XX MALE SYNDROME. A CASE REPORT.CULLEN M; GREALLY M; GREALLY J et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 10; NO 2; PP. 73-76; BIBL. 10 REF.Article

L'ANTIGENE H-Y ET SA MISE EN EVIDENCE CHEZ DES HOMMES 46, XX.TOUS J; POCHAT D; NOEL B et al.1978; REV. FR. ENDOCRINOL. CLIN.; FR.; DA. 1978; VOL. 19; NO 1; PP. 49-54; BIBL. 11 REF.Article

DAS XX-MANN-SYNDROM. PATHOGENESE UND BEITRAG ZU DEN TEHLERMOEGLICHKEITEN DER DIAGNOSE = LE SYNDROME XX MALE. PATHOGENESE ET CONTRIBUTION AUX POSSIBILITES D'ERREUR DE DIAGNOSTICREHDER H; BRUHL P; SETH PK et al.1975; UROLOGE, A; DTSCH.; DA. 1975; VOL. 14; NO 4; PP. 182-186; ABS. ANGL.; BIBL. 28 REF.Article

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RECESSIVE SEX-DETERMINING GENES IN HUMAN XX MALE SYNDROME.DE LA CHAPELLE A; KOO GC; WACHTEL SS et al.1978; CELL; USA; DA. 1978; VOL. 15; NO 3; PP. 837-842; BIBL. 20 REF.Article

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INHERITED MALE PSEUDOHERMAPHRODITISM DUE TO GONADOTROPHIN UNRESPONSIVENESSPEREZ PALACIOS G; SCAGLIA HE; KOFMAN ALFARO S et al.1981; ACTA ENDOCRINOL. (KBH.); ISSN 0001-5598; DNK; DA. 1981; VOL. 98; NO 1; PP. 148-155; BIBL. 17 REF.Article

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