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1
Early impact of X‐ and Y‐chromosome variations (XXX, XXY, XYY) on social communication and social emotional development in 1–2‐year‐old children
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Early impact of X‐ and Y‐chromosome variations (XXX, XXY, XYY) on social communication and social emotional development in 1–2‐year‐old children

Bouw, Nienke ; Swaab, Hanna ; Tartaglia, Nicole ; Jansen, Anna C. ; Rijn, Sophie

American journal of medical genetics. Part A, 2022-07, Vol.188 (7), p.1943-1953 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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2
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review
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Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review

LEGGETT, VICTORIA ; JACOBS, PATRICIA ; NATION, KATE ; SCERIF, GAIA ; BISHOP, DOROTHY V M

Developmental medicine and child neurology, 2010-02, Vol.52 (2), p.119-129 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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3
Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX
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Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX

van Rijn, S. ; Swaab, H.

Genes, brain and behavior, 2015-02, Vol.14 (2), p.200-208 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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4
Impact of tumor location on medulloblastoma subtyping and treatment (Commentary on teo et al., page xxx)
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Impact of tumor location on medulloblastoma subtyping and treatment (Commentary on teo et al., page xxx)

Robinson, Giles W.

Pediatric blood & cancer, 2013-09, Vol.60 (9), p.1393-1394 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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5
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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6
Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes
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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
Presentation and Outcomes of C4d‐Negative Antibody‐Mediated Rejection After Kidney Transplantation
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Presentation and Outcomes of C4d‐Negative Antibody‐Mediated Rejection After Kidney Transplantation

Orandi, B. J. ; Alachkar, N. ; Kraus, E. S. ; Naqvi, F. ; Lonze, B. E. ; Lees, L. ; Van Arendonk, K. J. ; Wickliffe, C. ; Bagnasco, S. M. ; Zachary, A. A. ; Segev, D. L. ; Montgomery, R. A.

American journal of transplantation, 2016-01, Vol.16 (1), p.213-220 [Periódico revisado por pares]

United States

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8
Validation of an Objective Assessment Tool for Tonsillectomy in Otolaryngology Resident Training
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Validation of an Objective Assessment Tool for Tonsillectomy in Otolaryngology Resident Training

Jakubowski, Luke ; Leader, Brittany A. ; Ishman, Stacey L. ; Chun, Robert ; Tarima, Sergey S. ; Parikh, Sanjay ; Skinner, Margaret ; Thorne, Marc ; Weatherly, Robert ; Wiet, Gregory ; Brown, David J.

The Laryngoscope, 2021-02, Vol.131 (2), p.E359-E366 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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9
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
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Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18

Chen, Chih‐Ping ; Chern, Schu‐Rern ; Yeh, Li‐Fan ; Chen, Wen‐Lin ; Chen, Li‐Feng ; Wang, Wayseen

Prenatal diagnosis, 2000-09, Vol.20 (9), p.750-753 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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10
47,XXX male: A clinical and molecular study
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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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