Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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The behavioral profile of children aged 1–5 years with sex chromosome trisomy (47,XXX, 47,XXY, 47,XYY)Urbanus, Evelien ; Swaab, Hanna ; Tartaglia, Nicole ; Cordeiro, Lisa ; Rijn, SophieAmerican journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.444-455Hoboken, USA: John Wiley & Sons, IncTexto completo disponível |
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2 |
Material Type: Artigo
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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 childrenBouw, Nienke ; Swaab, Hanna ; Tartaglia, Nicole ; Jansen, Anna C. ; Rijn, SophieAmerican journal of medical genetics. Part A, 2022-07, Vol.188 (7), p.1943-1953 [Periódico revisado por pares]Hoboken, USA: John Wiley & Sons, IncTexto completo disponível |
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3 |
Material Type: Artigo
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X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's SyndromeLiu, Ke ; Kurien, Biji T. ; Zimmerman, Sarah L. ; Kaufman, Kenneth M. ; Taft, Diana H. ; Kottyan, Leah C. ; Lazaro, Sara ; Weaver, Carrie A. ; Ice, John A. ; Adler, Adam J. ; Chodosh, James ; Radfar, Lida ; Rasmussen, Astrid ; Stone, Donald U. ; Lewis, David M. ; Li, Shibo ; Koelsch, Kristi A. ; Igoe, Ann ; Talsania, Mitali ; Kumar, Jay ; Maier‐Moore, Jacen S. ; Harris, Valerie M. ; Gopalakrishnan, Rajaram ; Jonsson, Roland ; Lessard, James A. ; Lu, Xianglan ; Gottenberg, Jacques‐Eric ; Anaya, Juan‐Manuel ; Cunninghame‐Graham, Deborah S. ; Huang, Andrew J. W. ; Brennan, Michael T. ; Hughes, Pamela ; Illei, Gabor G. ; Miceli‐Richard, Corinne ; Keystone, Edward C. ; Bykerk, Vivian P. ; Hirschfield, Gideon ; Xie, Gang ; Ng, Wan‐Fai ; Nordmark, Gunnel ; Eriksson, Per ; Omdal, Roald ; Rhodus, Nelson L. ; Rischmueller, Maureen ; Rohrer, Michael ; Segal, Barbara M. ; Vyse, Timothy J. ; Wahren‐Herlenius, Marie ; Witte, Torsten ; Pons‐Estel, Bernardo ; Alarcón‐Riquelme, Marta E. ; Guthridge, Joel M. ; James, Judith A. ; Lessard, Christopher J. ; Kelly, Jennifer A. ; Thompson, Susan D. ; Gaffney, Patrick M. ; Montgomery, Courtney G. ; Edberg, Jeffrey C. ; Kimberly, Robert P. ; Alarcón, Graciela S. ; Langefeld, Carl L. ; Gilkeson, Gary S. ; Kamen, Diane L. ; Tsao, Betty P. ; Joseph McCune, W. ; Salmon, Jane E. ; Merrill, Joan T. ; Weisman, Michael H. ; Wallace, Daniel J. ; Utset, Tammy O. ; Bottinger, Erwin P. ; Amos, Christopher I. ; Siminovitch, Katherine A. ; Mariette, Xavier ; Sivils, Kathy L. ; Harley, John B. ; Hal Scofield, R.Arthritis & rheumatology (Hoboken, N.J.), 2016-05, Vol.68 (5), p.1290-1300 [Periódico revisado por pares]United States: Wiley Subscription Services, IncTexto completo disponível |
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4 |
Material Type: Artigo
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Epigenetic and transcriptomic consequences of excess X‐chromosome material in 47,XXX syndrome—A comparison with Turner syndrome and 46,XX femalesNielsen, Morten Muhlig ; Trolle, Christian ; Vang, Søren ; Hornshøj, Henrik ; Skakkebæk, Anne ; Hedegaard, Jakob ; Nordentoft, Iver ; Pedersen, Jakob Skou ; Gravholt, Claus HøjbjergAmerican journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.279-293Hoboken, USA: John Wiley & Sons, IncTexto completo disponível |
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5 |
Material Type: Artigo
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Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic reviewLEGGETT, VICTORIA ; JACOBS, PATRICIA ; NATION, KATE ; SCERIF, GAIA ; BISHOP, DOROTHY V MDevelopmental medicine and child neurology, 2010-02, Vol.52 (2), p.119-129 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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6 |
Material Type: Artigo
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False‐negative trisomy 18 non‐invasive prenatal test result due to 48,XXX,+18 placental mosaicismGao, Y. ; Stejskal, D. ; Jiang, F. ; Wang, W.Ultrasound in obstetrics & gynecology, 2014-04, Vol.43 (4), p.477-478 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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7 |
Material Type: Artigo
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A case‐control study of brain structure and behavioral characteristics in 47,XXX syndromeLenroot, R. K. ; Blumenthal, J. D. ; Wallace, G. L. ; Clasen, L. S. ; Lee, N. R. ; Giedd, J. N.Genes, brain and behavior, 2014-11, Vol.13 (8), p.841-849 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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8 |
Material Type: Artigo
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Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre studyGruchy, Nicolas ; Blondeel, Eleonore ; Le Meur, Nathalie ; Joly-Hélas, Géraldine ; Chambon, Pascal ; Till, Marianne ; Herbaux, Martine ; Vigouroux-Castera, Adeline ; Coussement, Aurélie ; Lespinasse, James ; Amblard, Florence ; Jimenez Pocquet, Mélanie ; Lebel-Roy, Camille ; Carré-Pigeon, Frédérique ; Flori, Elisabeth ; Mugneret, Francine ; Jaillard, Sylvie ; Yardin, Catherine ; Harbuz, Radu ; Collonge-Rame, Marie-Agnès ; Vago, Philippe ; Valduga, Mylène ; Leporrier, Nathalie ; Vialard, FrançoisPrenatal diagnosis, 2016-06, Vol.36 (6), p.523-529 [Periódico revisado por pares]England: Blackwell Publishing LtdTexto completo disponível |
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9 |
Material Type: Artigo
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Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXXvan Rijn, S. ; Swaab, H.Genes, brain and behavior, 2015-02, Vol.14 (2), p.200-208 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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10 |
Material Type: Artigo
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A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21Li, Jin ; Xie, Mingshui ; Wang, Fang ; Ma, Jianhong ; Li, Jiafu ; Chen, Chen ; Li, Zhimin ; Wang, Juan ; Zhang, Yuanzhen ; Li, YirongMolecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1279-n/a [Periódico revisado por pares]United States: John Wiley & Sons, IncTexto completo disponível |