Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
---|---|---|---|
1 |
Material Type: Artigo
|
![]() |
Sex chromosome aneuploidies and fertility: 47,XXY, 47,XYY, 47,XXX and 45,X/47,XXXRogol, Alan DEndocrine Connections, 2023-08, Vol.12 (9), p.1-10 [Periódico revisado por pares]England: Bioscientifica LtdTexto completo disponível |
2 |
Material Type: Artigo
|
![]() |
A review of trisomy X (47,XXX)Tartaglia, Nicole R ; Howell, Susan ; Sutherland, Ashley ; Wilson, Rebecca ; Wilson, LennieOrphanet journal of rare diseases, 2010-05, Vol.5 (1), p.8-8, Article 8 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
3 |
Material Type: Artigo
|
![]() |
Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case reportLiang, Dong ; Han, Minmin ; Xu, Linxin ; Ren, Yi ; Zhang, Yi ; Yin, Jianhong ; Yang, Jing ; Liu, YunfengMedicine (Baltimore), 2022-10, Vol.101 (43), p.e31443-e31443 [Periódico revisado por pares]United States: Lippincott Williams & WilkinsTexto completo disponível |
4 |
Material Type: Artigo
|
![]() |
Detection of VEGF-A(xxx)b isoforms in human tissuesBates, 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 JPloS one, 2013, Vol.8 (7), p.e68399 [Periódico revisado por pares]United States: Public Library of Science (PLoS)Texto completo disponível |
5 |
Material Type: Artigo
|
![]() |
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort studyBerglund, Agnethe ; Viuff, Mette Hansen ; Skakkebæk, Anne ; Chang, Simon ; Stochholm, Kirstine ; Gravholt, Claus HøjbjergOrphanet journal of rare diseases, 2019-01, Vol.14 (1), p.16-16, Article 16 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
6 |
Material Type: Artigo
|
![]() |
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 |
7 |
Material Type: Artigo
|
![]() |
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 |
8 |
Material Type: Artigo
|
![]() |
Altered subcortical and cortical brain morphology in adult women with 47,XXX: a 7-Tesla magnetic resonance imaging studySerrarens, Chaira ; Otter, Maarten ; Campforts, Bea C M ; Stumpel, Constance T R M ; Jansma, Henk ; van Amelsvoort, Thérèse A M J ; Vingerhoets, ClaudiaJournal of neurodevelopmental disorders, 2022-02, Vol.14 (1), p.14-14, Article 14 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
9 |
Material Type: Artigo
|
![]() |
Healthcare and support experiences of adolescents and young adults diagnosed with 47,XXY, 47,XXX, and 48,XXYYAhlawat, 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 HeidelbergTexto completo disponível |
10 |
Material Type: Artigo
|
![]() |
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 |