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1
Epigenetic and transcriptomic consequences of excess X‐chromosome material in 47,XXX syndrome—A comparison with Turner syndrome and 46,XX females
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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 females

Nielsen, Morten Muhlig ; Trolle, Christian ; Vang, Søren ; Hornshøj, Henrik ; Skakkebæk, Anne ; Hedegaard, Jakob ; Nordentoft, Iver ; Pedersen, Jakob Skou ; Gravholt, Claus Højbjerg

American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.279-293

Hoboken, USA: John Wiley & Sons, Inc

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2
X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome
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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 Syndrome

Liu, 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, Inc

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3
Detection of VEGF-A(xxx)b isoforms in human tissues
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Detection of VEGF-A(xxx)b isoforms in human tissues

Bates, David O ; Mavrou, Athina ; Qiu, Yan ; Carter, James G ; Hamdollah-Zadeh, Maryam ; Barratt, Shaney ; Gammons, Melissa V ; Millar, Ann B ; Salmon, Andrew H J ; Oltean, Sebastian ; Harper, Steven J

PloS one, 2013, Vol.8 (7), p.e68399 [Periódico revisado por pares]

United States: Public Library of Science (PLoS)

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4
A review of trisomy X (47,XXX)
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A review of trisomy X (47,XXX)

Tartaglia, Nicole R ; Howell, Susan ; Sutherland, Ashley ; Wilson, Rebecca ; Wilson, Lennie

Orphanet journal of rare diseases, 2010-05, Vol.5 (1), p.8-8, Article 8 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case report
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Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case report

Liang, Dong ; Han, Minmin ; Xu, Linxin ; Ren, Yi ; Zhang, Yi ; Yin, Jianhong ; Yang, Jing ; Liu, Yunfeng

Medicine (Baltimore), 2022-10, Vol.101 (43), p.e31443-e31443 [Periódico revisado por pares]

United States: Lippincott Williams & Wilkins

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6
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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7
Healthcare and support experiences of adolescents and young adults diagnosed with 47,XXY, 47,XXX, and 48,XXYY
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Healthcare and support experiences of adolescents and young adults diagnosed with 47,XXY, 47,XXX, and 48,XXYY

Ahlawat, Nivedita ; Elliott, Kathryn ; Ormond, Kelly E. ; Allyse, Megan A. ; Riggan, Kirsten A.

Journal of community genetics, 2024-02, Vol.15 (1), p.75-83 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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8
Limits to sustained energy intake. XXX. Constraint or restraint? Manipulations of food supply show peak food intake in lactation is constrained
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Limits to sustained energy intake. XXX. Constraint or restraint? Manipulations of food supply show peak food intake in lactation is constrained

Zhao, Zhi-Jun ; Derous, Davina ; Gerrard, Abby ; Wen, Jing ; Liu, Xue ; Tan, Song ; Hambly, Catherine ; Speakman, John R

Journal of experimental biology, 2020-04, Vol.223 (Pt 8) [Periódico revisado por pares]

England

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9
A cross-sectional study of early language abilities in children with sex chromosome trisomy (XXY, XXX, XYY) aged 1-6 years
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A cross-sectional study of early language abilities in children with sex chromosome trisomy (XXY, XXX, XYY) aged 1-6 years

Urbanus, Evelien ; Swaab, Hanna ; Tartaglia, Nicole ; Boada, Richard ; van Rijn, Sophie

Child neuropsychology, 2022-02, Vol.28 (2), p.171-196 [Periódico revisado por pares]

England: Routledge

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10
A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome
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A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome

Lenroot, 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 Ltd

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