Congenital heart disease in the 48,XXYY syndromeMESCHEDE, D; NEKARDA, T; KECECIOGLU, D et al.Clinical genetics. 1995, Vol 48, Num 2, pp 100-102, issn 0009-9163Article

AGRESSIVITE, DEBILITE MENTALE ET EPILEPSIE CHEZ UN SUJET DE CARYOTYPE 47XYY/48XXYYBENEZECH M; NOEL B; MESSAGER A et al.1972; REV. NEUROPSYCHIATR. INFANT. HYG. MENTALE ENFANCE; FR.; DA. 1972; VOL. 20; NO 10; PP. 773-775; ABS. ANGL. ALLEM. ESP.; BIBL. 8REF.Serial Issue

STIGMATE "MONGOLOIDI" NELLA DIAGNOSI IN ETA PEDIATRICA DEI SOGGETTI A CORREDO 48,XXYY = STIGMATES "MONGOLOIDES" DANS LE DIAGNOSTIC CHEZ L'ENFANT DES SUJETS AVEC FORMULE 48,XXYYCHELI E; MONTEFUSCO R; BARONCINI A et al.1978; MINERVA PEDIATR.; ITA; DA. 1978; VOL. 30; NO 14; PP. 1171-1178; ABS. ENG; BIBL. 19 REF.Article

Jeunes enfants 48 XXYY. Difficultés d'établissement du diagnostic = Young children 48 XXYY. Difficult diagnosisGENEIX, A; PERISSEL, B; TURCHINI, M. F et al.Bordeaux médical. 1985, Vol 18, Num 9, pp 305-306, issn 0021-7867Article

A SEX CHROMATIN AND Y BODY SURVEY OF TORONTO NEWBORNSBELL AG; COREX PN.1974; CANAD. J. GENET. CYTOL.; CANADA; DA. 1974; VOL. 16; NO 2; PP. 239-250; BIBL. 22REF.Article

CASE STUDIES OF THREE "XXYY" CHILDREN. = OBSERVATIONS DE 3 ENFANTS "XXYY"GARVEY M; KELLETT B.1975; BRIT. J. DISORD. COMMUNIC.; G.B.; DA. 1975; VOL. 10; NO 1; PP. 17-30; BIBL. 22 REF.Article

48, XXYY-Syndrom bei einem Knaben mit essentiellem Tremor : Vergleich mit 120 Fällen aus der Literature = 48, XXYY syndrome in a boy with essentiel tremor : comparism with 120 others casesDONATI, F; GASSER, S; MULLIS, P et al.Monatsschrift für Kinderheilkunde. 1992, Vol 140, Num 4, pp 216-219, issn 0026-9298Conference Paper

PROBLEMI DI INQUADRAMENTO CLINICO DELLA SINDROME 48, XXYY IN ETA PEDIATRICA = PROBLEMES DE L'ENCADREMENT CLINIQUE DU SYNDROME 48, XXYY CHEZ L'ENFANTVIGI V; GUERRINI P; PINCA A et al.1980; CLIN. PEDIATR.; ITA; DA. 1980; VOL. 62; NO 1; PP. 10-15; ABS. ENG; BIBL. 7 REF.Article

Social deficits in male children and adolescents with sex chromosome aneuploidy: A comparison of XXY, XYY, and XXYY syndromesCORDEIRO, Lisa; TARTAGLIA, Nicole; ROELTGEN, David et al.Research in developmental disabilities (Print). 2012, Vol 33, Num 4, pp 1254-1263, issn 0891-4222, 10 p.Article

Attention-Deficit Hyperactivity Disorder Symptoms in Children and Adolescents with Sex Chromosome Aneuploidy: XXY, XXX, XYY, and XXYYTARTAGLIA, Nicole R; AYARI, Natalie; HUTAFF-LEE, Christa et al.Journal of developmental and behavioral pediatrics. 2012, Vol 33, Num 4, pp 309-318, issn 0196-206X, 10 p.Article

48, XXYY syndrome associated with ethylenediaminetetraacetic acid (EDTA)-dependent pseudothrombocytopeniaKODAMA, T; IMAI, H; NAKAMOTO, Y et al.Internal medicine : (Tokyo). 1992, Vol 31, Num 1, pp 143-146Article

DERMATOGLIFOS INFRECUENTES EN 2 PACIENTES. XXYY. = DERMATOGLYPHES RARES CHEZ 2 MALADES XXYYFERRO DELGADO MT; GARCIA SAGREDO JM.1977; REV. CLIN. ESP.; ESP.; DA. 1977; VOL. 146; NO 5; PP. 285-286; BIBL. 8 REF.Article

ULTRASTRUCTURE OF LEYDIG CELLS IN KLINEFELTER'S SYNDROME WITH 48, XXYY KARYOTYPENISTAL M; PANIAGUA R; LOPEZ PAJARES I et al.1978; VIRCHOWS ARCH., B; DEU; DA. 1978; VOL. 28; NO 1; PP. 39-46; BIBL. 25 REF.Article

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

Endocrine function in a 48,XXYY adult with type 2 diabetes : case report with a review of the literatureDUBOIS, S; ILLOUZ, F; PINSON, L et al.Annales d'endocrinologie. 2007, Vol 68, Num 5, pp 384-388, issn 0003-4266, 5 p.Article

GENETIC AND ENDOCRINE FINDINGS IN A 48,XXYY MALEBLOOMGARDEN ZT; DELOZIER CD; COHEN MP et al.1980; J. CLIN. ENDOCRINOL. METABOL.; USA; DA. 1980; VOL. 50; NO 4; PP. 740-743; BIBL. 24 REF.Article

The 48,XXYY syndrome follow-up data on clinical characteristics and psychological findings in a patientsBORGHGRAEF, M; FRYNS, J. P; VAN DEN BERGHE, H et al.Genetic counseling. 1991, Vol 2, Num 2, pp 103-108Article

Tremor in 48,XXYY SyndromeTARTAGLIA, Nicole; BORODYANSKYA, Mariya; HALL, Deborah A et al.Movement disorders. 2009, Vol 24, Num 13, pp 2001-2007, issn 0885-3185, 7 p.Article

48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndromeTARTAGLIA, Nicole; AYARI, Natalie; HOWELL, Susan et al.Acta paediatrica (Oslo). 2011, Vol 100, Num 6, pp 851-860, issn 0803-5253, 10 p.Conference Paper

Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXYVISOOTSAK, Jeannie; ROSNER, Beth; DYKENS, Elisabeth et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 11, pp 1198-1203, issn 1552-4825, 6 p.Article

A New Look at XXYY Syndrome : Medical and Psychological FeaturesTARTAGLIA, Nicole; DAVIS, Shanlee; HANSEN, Robin et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 12, pp 1509-1522, issn 1552-4825, 14 p.Article

SOCIAL FUNCTION IN MULTIPLE X AND Y CHROMOSOME DISORDERS: XXY, XYY, XXYY, XXXYVISOOTSAK, Jeannie; GRAHAM, John M.Developmental disabilities research reviews. 2009, Vol 15, Num 4, pp 328-332, issn 1940-5510, 5 p.Article