Clinical and molecular features of Ewing sarcoma in a patient with triple-X syndromePATINO-GARCIA, A; LOPEZ DE MESA, R; DE ALAVA, E et al.Cancer genetics and cytogenetics. 1999, Vol 113, Num 2, pp 188-190, issn 0165-4608Article

Dysgerminoma of the ovary in a patient with triple-X syndromeKEMP, B; HAUPTMANN, S; SCHRÖDER, W et al.International journal of gynaecology and obstetrics. 1995, Vol 50, Num 1, pp 51-53, issn 0020-7292Article

Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disordersGOSWAMI, Ravinder; GOSWAMI, Deepti; KABRA, Madhulika et al.Fertility and sterility. 2003, Vol 80, Num 4, pp 1052-1054, issn 0015-0282, 3 p.Article

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

Triple X Syndrome with Rare Phenotypic PresentationJAGADEESH, Sujatha; JABEEN, Gazala; BHAT, Lathaa et al.Indian journal of pediatrics. 2008, Vol 75, Num 6, pp 629-631, issn 0019-5456, 3 p.Article

Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the LiteratureBAGCI, Soyhan; MÜLLER, Andreas; FRANZ, Axel et al.Fetal diagnosis and therapy. 2010, Vol 27, Num 2, pp 113-117, issn 1015-3837, 5 p.Article