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Refinado por: Base de dados/Biblioteca: Wiley Online Library All Journals remover xxx: xxx remover EZB Free E-Journals remover
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1
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review
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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2
Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX
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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3
Presentation and Outcomes of C4d‐Negative Antibody‐Mediated Rejection After Kidney Transplantation
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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4
X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization
X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization
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X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterization

Kushima, Itaru ; Aleksic, Branko ; Kimura, Hiroki ; Nakatochi, Masahiro ; Lo, Tzuyao ; Ikeda, Masashi ; Arai, Makoto ; Hashimoto, Ryota ; Numata, Shusuke ; Okamura, Yasunobu ; Obara, Taku ; Inada, Toshiya ; Ozaki, Norio

Psychiatry and clinical neurosciences, 2022-12, Vol.76 (12), p.667-673 [Periódico revisado por pares]

Melbourne: John Wiley & Sons Australia, Ltd

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5
Chromosomes and causation of human cancer and leukemia XXX. Banding studies of primary intestinal tumors
Chromosomes and causation of human cancer and leukemia XXX. Banding studies of primary intestinal tumors
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Chromosomes and causation of human cancer and leukemia XXX. Banding studies of primary intestinal tumors

Sonta, Shin‐Ichi ; Sandberg, Avery A.

Cancer, 1978-01, Vol.41 (1), p.164-173 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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6
Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage
Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage
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Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage

Liu, S. ; Song, L. ; Cram, D. S. ; Xiong, L. ; Wang, K. ; Wu, R. ; Liu, J. ; Deng, K. ; Jia, B. ; Zhong, M. ; Yang, F.

Ultrasound in obstetrics & gynecology, 2015-10, Vol.46 (4), p.472-477 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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7
Non‐invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta‐analysis of diagnostic test accuracy studies
Non‐invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta‐analysis of diagnostic test accuracy studies
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Non‐invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta‐analysis of diagnostic test accuracy studies

Soukkhaphone, Bounhome ; Lindsay, Carmen ; Langlois, Sylvie ; Little, Julian ; Rousseau, Francois ; Reinharz, Daniel

Molecular Genetics & Genomic Medicine, 2021-05, Vol.9 (5), p.e1654-n/a [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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8
Health care resource utilization before and after perampanel initiation among patients with epilepsy in the United States
Health care resource utilization before and after perampanel initiation among patients with epilepsy in the United States
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Health care resource utilization before and after perampanel initiation among patients with epilepsy in the United States

Faught, Edward ; Laliberté, François ; Wang, Zhixiao ; Barghout, Victoria ; Haider, Batool ; Lejeune, Dominique ; Germain, Guillaume ; Choi, Jiyoon ; Wagh, Aneesha ; Duh, Mei Sheng

Epilepsia (Copenhagen), 2017-10, Vol.58 (10), p.1742-1748 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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9
Eosinophilic esophagitis in individuals with sex chromosome aneuploidies: Clinical presentations and management implications
Eosinophilic esophagitis in individuals with sex chromosome aneuploidies: Clinical presentations and management implications
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Eosinophilic esophagitis in individuals with sex chromosome aneuploidies: Clinical presentations and management implications

Howell, Susan ; Buchanan, Catherine ; Davis, Shanlee M. ; Miyazawa, Heather ; Furuta, Glenn T. ; Tartaglia, Nicole R. ; Nguyen, Nathalie

Molecular genetics & genomic medicine, 2021-12, Vol.9 (12), p.e1833-n/a [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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10
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

Simpson, Nuala H ; Addis, Laura ; Brandler, William M ; Slonims, Vicky ; Clark, Ann ; Watson, Jocelynne ; Scerri, Thomas S ; Hennessy, Elizabeth R ; Bolton, Patrick F ; Conti‐Ramsden, Gina ; Fairfax, Benjamin P ; Knight, Julian C ; Stein, John ; Talcott, Joel B ; O'Hare, Anne ; Baird, Gillian ; Paracchini, Silvia ; Fisher, Simon E ; Newbury, Dianne F ; Consortium, SLI

Developmental medicine and child neurology, 2014-04, Vol.56 (4), p.346-353 [Periódico revisado por pares]

England: BlackWell Publishing Ltd

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