Literature DB >> 12784313

Clinical findings and phenotype in a toddler with 48,XXYY syndrome.

Osman Demirhan.   

Abstract

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Year:  2003        PMID： 12784313     DOI： 10.1002/ajmg.a.20015

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  6 in total

1.  48,XXYY in a General Adult Psychiatry Department.

Authors:  Nuno Borja-Santos; Bruno Trancas; Pilar Santos Pinto; Bárbara Lopes; António Gamito; Sandra Almeida; Berta Ferreira; Antonio Luengo; Carlos Vieira; Jorge Martinho; Bruno Pereira; Graça Cardoso
Journal:  Psychiatry (Edgmont)       Date:  2010-03

2.  A rare sex chromosome aneuploidy: 48,XXYY syndrome.

Authors:  Tahir Atik; Özgür Çoğulu; Ferda Özkınay
Journal:  Turk Pediatri Ars       Date:  2016-06-01

Review 3.  48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome.

Authors:  Nicole Tartaglia; Natalie Ayari; Susan Howell; Cheryl D'Epagnier; Philip Zeitler
Journal:  Acta Paediatr       Date:  2011-04-08       Impact factor: 2.299

Review 4.  Effects of sex chromosome aneuploidies on brain development: evidence from neuroimaging studies.

Authors:  Rhoshel K Lenroot; Nancy Raitano Lee; Jay N Giedd
Journal:  Dev Disabil Res Rev       Date:  2009

5.  A new look at XXYY syndrome: medical and psychological features.

Authors:  Nicole Tartaglia; Shanlee Davis; Alison Hench; Sheela Nimishakavi; Renee Beauregard; Ann Reynolds; Laura Fenton; Lindsey Albrecht; Judith Ross; Jeannie Visootsak; Robin Hansen; Randi Hagerman
Journal:  Am J Med Genet A       Date:  2008-06-15       Impact factor: 2.802

6.  Rare 48, XYYY syndrome: case report and review of the literature.

Authors:  Maryam Abedi; Arash Salmaninejad; Ebrahim Sakhinia
Journal:  Clin Case Rep       Date:  2017-12-07
  6 in total

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