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1
Attention-Deficit Hyperactivity Disorder Symptoms in Children and Adolescents with Sex Chromosome Aneuploidy: XXY, XXX, XYY, and XXYY
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Attention-Deficit Hyperactivity Disorder Symptoms in Children and Adolescents with Sex Chromosome Aneuploidy: XXY, XXX, XYY, and XXYY

TARTAGLIA, Nicole R ; AYARI, Natalie ; HUTAFF-LEE, Christa ; BOADA, Richard

Journal of developmental and behavioral pediatrics, 2012-05, Vol.33 (4), p.309-318 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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2
The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination
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The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination

MacDonald, M. ; Hassold, T. ; Harvey, J. ; Wang, L.H. ; Morton, N.E. ; Jacobs, P.

Human molecular genetics, 1994-08, Vol.3 (8), p.1365-1371 [Periódico revisado por pares]

Oxford: Oxford University Press

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3
Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful knee
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Artigo
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Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful knee

MEENAGH, G ; FILIPPUCCI, E ; DELLE SEDIE, A ; IAGNOCCO, A ; SCIRE, C. A ; RIENTE, L ; MONTECUCCO, C ; VALESINI, G ; BOMBARDIERI, S ; GRASSI, W

Clinical and experimental rheumatology, 2010-11, Vol.28 (6), p.803-805 [Periódico revisado por pares]

Pisa: Clinical and Experimental Rheumatology

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4
Long-term survival in a 69,XXX triploid premature infant
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Artigo
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Long-term survival in a 69,XXX triploid premature infant

Takabachi, Noriko ; Nishimaki, Shigeru ; Omae, Mari ; Okuda, Mika ; Fujita, Shujiro ; Ishida, Fumihiko ; Horiguchi, Haruko ; Seki, Kazuo ; Takahashi, Tsuneo ; Yokota, Shumpei

American journal of medical genetics. Part A, 2008-06, Vol.146A (12), p.1618-1621 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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5
Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events
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Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events

Szalai, A. J. ; Alarcón, G. S. ; Calvo-Alén, J. ; Toloza, S. M. A. ; McCrory, M. A. ; Edberg, J. C. ; McGwin, G. ; Bastian, H. M. ; Fessler, B. J. ; Vilá, L. M. ; Kimberly, R. P. ; Reveille, J. D.

Rheumatology (Oxford, England), 2005-07, Vol.44 (7), p.864-868 [Periódico revisado por pares]

Oxford: Oxford University Press

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6
Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes
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Artigo
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Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes

Patwardhan, Anil J. ; Brown, Wendy E. ; Bender, Bruce G. ; Linden, Mary G. ; Eliez, Stephan ; Reiss, Allan L.

American journal of medical genetics, 2002-01, Vol.114 (1), p.93-98 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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7
Doctors’ experiences of adverse events in secondary care: the professional and personal impact
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Artigo
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Doctors’ experiences of adverse events in secondary care: the professional and personal impact

Harrison, Reema ; Lawton, Rebecca ; Stewart, Kevin

Clinical medicine (London, England), 2014-12, Vol.14 (6), p.585-590 [Periódico revisado por pares]

London: Elsevier Ltd

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8
The parental origin of the extra X chromosome in 47,XXX females
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Artigo
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The parental origin of the extra X chromosome in 47,XXX females

MAY, K. M ; JACOBS, P. A ; LEE, M ; RATCLIFFE, S ; ROBINSON, A ; NIELSEN, J ; HASSOLD, T. J

American journal of human genetics, 1990-04, Vol.46 (4), p.754-761 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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9
Azoospermia in a 46,xx/47,xxx phenotypic male
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Artigo
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Azoospermia in a 46,xx/47,xxx phenotypic male

Cooper, Christopher S. ; Sandlow, Jay I.

Urology (Ridgewood, N.J.), 1996-12, Vol.48 (6), p.947-948 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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10
47,XXX male: A clinical and molecular study
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Artigo
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47,XXX male: A clinical and molecular study

Ogata, Tsutomu ; Matsuo, Mari ; Muroya, Koji ; Koyama, Yasuhiro ; Fukutani, Keiko

American journal of medical genetics, 2001-02, Vol.98 (4), p.353-356 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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