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ArticlesFull Text
Fraccaro Syndrome (49,XXXXY): Case study in antenatal and postnatal from South Indian patients, an awareness to the human society
Author / Creator:Flora Bai, B. ; Sujithra, A. ; Padhiar, C. ; Arjun, P. ; Wilson Aruni Santhosh Kumar, A.
Publisher:Lucknow: Triveni Enterprises
Journal title:Journal of environmental biology, 2024-03, Vol.45 (2), p.125-129
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ArticlesPeer ReviewedFull Text
Fraccaro Syndrome: Report of Two Iranian Cases: An Infant and an Adult in A Family Fraccaro Syndrome: Report of Two Iranian Cases: An Infant and an Adult in A Family
Author / Creator:Fatemeh Hadipour ; Yousef Shafeghati ; Eiman Bagherizadeh ; Farkhondeh Behjati ; Zahra Hadipour
Publisher:Tehran University of Medical Sciences
Journal title:Acta medica Iranica, 2013-12, Vol.51 (12)
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ArticlesPeer ReviewedFull Text
Fraccaro syndrome: report of two Iranian cases: an infant and an adult in a family
Author / Creator:Hadipour, Fatemeh ; Shafeghati, Yousef ; Bagherizadeh, Eiman ; Behjati, Farkhondeh ; Hadipour, Zahra
Publisher:Iran: Tehran University of Medical Sciences
Journal title:Acta medica Iranica, 2013, Vol.51 (12), p.907
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Case Report of 49,XXXXY Syndrome: A Rare Variation of Klinefelter Syndrome With Seizure Disorder and ASD
Author / Creator:Shrestha, Ankit ; Parajuli, Biraj ; Pandit, Aakash
Publisher:England: John Wiley & Sons, Inc
Journal title:Clinical case reports, 2025-03, Vol.13 (3), p.e70257-n/a
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ArticlesPeer ReviewedFull Text
49,XXXXY syndrome: A case study and a systematic review of clinical features among the Iranian population
Author / Creator:Rajabzadeh, Mahboubeh ; Taheri, Nafiseh ; Jazayeri, Omid
Publisher:England: John Wiley & Sons, Inc
Journal title:Clinical case reports, 2022-09, Vol.10 (9), p.e6342-n/a
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ArticlesPeer ReviewedFull Text
48, XXXY/49, XXXXY mosaic: new neuroradiological features in an ultra-rare syndrome
Author / Creator:Milani, Donatella ; Bonarrigo, Francesca ; Avignone, Sabrina ; Triulzi, Fabio ; Esposito, Susanna
Publisher:England: BioMed Central
Journal title:Italian journal of pediatrics, 2015-07, Vol.41 (1), p.50-50, Article 50
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ArticlesPeer ReviewedFull Text
Leydig cell tumor in a patient with 49,XXXXY karyotype: a review of literature
Author / Creator:Maqdasy, Salwan ; Bogenmann, Laura ; Batisse-Lignier, Marie ; Roche, Béatrice ; Franck, Fréderic ; Desbiez, Françoise ; Tauveron, Igor
Publisher:England: BioMed Central Ltd
Journal title:Reproductive biology and endocrinology, 2015-07, Vol.13 (1), p.72-72, Article 72
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ArticlesPeer ReviewedFull Text
Cat Eye Syndrome with a Unique Liver and Dermatological Presentation
Author / Creator:Mansur, Maureen ; Jacob, Thomas J ; Wong, Helen ; Tarascin, Ilya
Publisher:United States: Springer Nature B.V
Journal title:Cureus, 2023-04, Vol.15 (4), p.e37142-e37142
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ArticlesPeer ReviewedFull Text
Parental Origin and Cell Stage Errors in X-Chromosome Polysomy 49, XXXXY
Author / Creator:Guzel, A ; Demirhan, O ; Pazarbasi, A ; Yuksel, B
Publisher:Sofia: Versita
Journal title:Balkan journal of medical genetics, 2009-01, Vol.12 (1), p.45-50
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ArticlesPeer ReviewedFull Text
High-risk ST-elevation acute coronary syndrome in a patient with multivessel coronary artery disease complicated by refractory cardiogenic shock undergoing complex percutaneous coronary revascularizat...
Author / Creator:Masiero, Giulia ; Pavei, Andrea ; Fraccaro, Chiara ; Napodano, Massimo ; Tarantini, Giuseppe
Publisher:Italy
Journal title:Giornale italiano di cardiologia (2006), 2018-06, Vol.19 (6), p.36-41S
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Contiguous Gene Syndromes Due to Deletions in the Distal Short Arm of the Human X Chromosome
Author / Creator:Ballabio, A. ; Bardoni, B. ; Carrozzo, R. ; Andria, G. ; Bick, D. ; Campbell, L. ; Hamel, B. ; Ferguson-Smith, M. A. ; Gimelli, G. ; Fraccaro, M. ; Maraschio, P. ; Zuffardi, O. ; Guioli, S. ; Camerino, G.
Publisher:Washington, DC: National Academy of Sciences of the United States of America
Journal title:Proceedings of the National Academy of Sciences - PNAS, 1989-12, Vol.86 (24), p.10001-10005
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ArticlesPeer ReviewedFull Text
47,XXY/48,XXXY/49,XXXXY mosaic with hydrocephaly: a case report and review of the literature
Author / Creator:Dueñas-Arias, Jesús E. ; Aguilar-Medina, Maribel ; Arámbula-Meraz, Eliakym ; Valenzuela-Camacho, Juliana B. ; Vega-Solano, Angelina ; Granados, Julio ; Ramos-Payán, Rosalío
Publisher:England: BioMed Central Ltd
Journal title:Journal of medical case reports, 2007-09, Vol.1 (1), p.94-94, Article 94
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Fraccaro Syndrome (49,XXXXY): Case study in antenatal and postnatal from South Indian patients, an awareness to the human society

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Fraccaro Syndrome: Report of Two Iranian Cases: An Infant and an Adult in A Family Fraccaro Syndrome: Report of Two Iranian Cases: An Infant and an Adult in A Family

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Fraccaro syndrome: report of two Iranian cases: an infant and an adult in a family

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Case Report of 49,XXXXY Syndrome: A Rare Variation of Klinefelter Syndrome With Seizure Disorder and ASD

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49,XXXXY syndrome: A case study and a systematic review of clinical features among the Iranian population

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48, XXXY/49, XXXXY mosaic: new neuroradiological features in an ultra-rare syndrome

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Leydig cell tumor in a patient with 49,XXXXY karyotype: a review of literature

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Cat Eye Syndrome with a Unique Liver and Dermatological Presentation

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Parental Origin and Cell Stage Errors in X-Chromosome Polysomy 49, XXXXY

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High-risk ST-elevation acute coronary syndrome in a patient with multivessel coronary artery disease complicated by refractory cardiogenic shock undergoing complex percutaneous coronary revascularizat...

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Contiguous Gene Syndromes Due to Deletions in the Distal Short Arm of the Human X Chromosome

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47,XXY/48,XXXY/49,XXXXY mosaic with hydrocephaly: a case report and review of the literature

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