PRENATAL MONITORING AND GENETIC COUNSELING IN A 47,XXX FEMALE WITH THE ORO-FACIAL DIGITAL SYNDROME, TYPE ICOHEN MM; CHARROW J; NADLER HL et al.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 4; PP. 649-650; BIBL. 2 REF.Article

, XXX KARYOTYPE OBTAINED BY AMNIOCENTESIS.LEVY DL; HOLLAND JB.1976; OBSTETR. AND GYNECOL.; U.S.A.; DA. 1976; VOL. 48; NO 2; PP. 233-234; BIBL. 5 REF.Article

XXX. SYNDROME ASSOCIATED WITH IMMUNOGLOBULIN DEFICIENCY AND EPILEPSYSILLS JA; BROWN JK; GRACE E et al.1978; J. PEDIATR.; USA; DA. 1978; VOL. 93; NO 3; PP. 469-471; BIBL. 8 REF.Article

Autoimmunity in a patient withe 47,XXX karyotypeMICHALAK, D. P; ZACUR, H. A; ROCK, J. A et al.Obstetrics and gynecology (New York. 1953). 1983, Vol 62, Num 5, pp 667-669, issn 0029-7844Article

THE DERMATOGLYPHICS OF A TORONTO SAMPLE OF CHILDREN WITH XXY, XXYY, AND XXX ANEUPLOIDIESHERECZKO TA; SIGMON BA.1980; AMER. J. PHYS. ANTHROPOL.; USA; DA. 1980; VOL. 52; NO 1; PP. 33-41; BIBL. 22 REF.Article

FETAL GONADAL HISTOLOGY IN XXXXY, XYY AND XXX SYNDROMESAUTIO HARMAINEN H; RAPOLA J; AULA P et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 1; PP. 1-5; BIBL. 11 REF.Article

47,XXX chromosome constitution, ovarian dysgenesis, and genito-urinary malformationSPEAR, G. S; PORTO, M.American journal of medical genetics. 1988, Vol 29, Num 3, pp 511-515, issn 0148-7299Article

PREGNANCY IN FIVE WOMEN WITH 45, X/46, XX AND 45, X/47, XXX GONADAL DYSGENESISSHOKEIR MHK.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 171-184; BIBL. 35 REF.Article

A case of 2-methylacetoacetyl CoA thiolase deficiency with coincidental chromosome abnormalitiesGRAY, R. G. F; LOWTHER, G. W; LITTLEWOOD, J. M et al.Journal of medical genetics. 1984, Vol 21, Num 5, issn 0022-2593, 397Article

MALIGNANT STROMAL TUMOUR OF THE OVARY WITH VIRILIZING EFFECTS IN AN XXX FEMALE WITH STREAK OVARIES: CLINICAL AND PATHOLOGICAL STUDIESKHOO SK; BUNTINE D.1980; AUSTRAL. NEW ZEAL. J. OBSTETR. GYNAECOL.; AUS; DA. 1980; VOL. 20; NO 2; PP. 123-128; BIBL. 11 REF.Article

FOLLOW-UP TILL AGE 3-4 OF UNSELECTED CHILDREN WITH SEX CHROMOSOME ABNORMALITIES.NIELSEN J; SILLESEN I.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 3; PP. 241-257; BIBL. 1 P. 1/2Article

47,XXX male: A clinical and molecular studyOGATA, Tsutomu; MATSUO, Mari; MUROYA, Koji et al.American journal of medical genetics. 2001, Vol 98, Num 4, pp 353-356, issn 0148-7299Article

Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosisLALATTA, Faustina; QUAGLIARINI, Donatella; NARETTO, Valeria Giorgia et al.European journal of pediatrics. 2010, Vol 169, Num 10, pp 1255-1261, issn 0340-6199, 7 p.Article

An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunctionANNEREN, G; ANDERSSON, M; PAGE, D. C et al.American journal of human genetics. 1987, Vol 41, Num 4, pp 594-604, issn 0002-9297Article