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Refinado por: Base de dados/Biblioteca: ROAD: Directory of Open Access Scholarly Resources remover xxx: xxx remover
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1
A review of trisomy X (47,XXX)
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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2
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
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Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study

Berglund, Agnethe ; Viuff, Mette Hansen ; Skakkebæk, Anne ; Chang, Simon ; Stochholm, Kirstine ; Gravholt, Claus Højbjerg

Orphanet journal of rare diseases, 2019-01, Vol.14 (1), p.16-16, Article 16 [Periódico revisado por pares]

England: BioMed Central Ltd

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3
Detection of VEGF-A(xxx)b isoforms in human tissues
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 rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
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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,+21

Li, Jin ; Xie, Mingshui ; Wang, Fang ; Ma, Jianhong ; Li, Jiafu ; Chen, Chen ; Li, Zhimin ; Wang, Juan ; Zhang, Yuanzhen ; Li, Yirong

Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1279-n/a [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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5
Altered subcortical and cortical brain morphology in adult women with 47,XXX: a 7-Tesla magnetic resonance imaging study
Altered subcortical and cortical brain morphology in adult women with 47,XXX: a 7-Tesla magnetic resonance imaging study
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Altered subcortical and cortical brain morphology in adult women with 47,XXX: a 7-Tesla magnetic resonance imaging study

Serrarens, Chaira ; Otter, Maarten ; Campforts, Bea C M ; Stumpel, Constance T R M ; Jansma, Henk ; van Amelsvoort, Thérèse A M J ; Vingerhoets, Claudia

Journal of neurodevelopmental disorders, 2022-02, Vol.14 (1), p.14-14, Article 14 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
Characterization and evolutionary implications of the triad Asp-Xxx-Glu in group II phosphopantetheinyl transferases
Characterization and evolutionary implications of the triad Asp-Xxx-Glu in group II phosphopantetheinyl transferases
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Characterization and evolutionary implications of the triad Asp-Xxx-Glu in group II phosphopantetheinyl transferases

Wang, Yue-Yue ; Li, Yu-Dong ; Liu, Jian-Bo ; Ran, Xin-Xin ; Guo, Yuan-Yang ; Ren, Ni-Ni ; Chen, Xin ; Jiang, Hui ; Li, Yong-Quan Jeltsch, Albert

PloS one, 2014-07, Vol.9 (7), p.e103031-e103031 [Periódico revisado por pares]

United States: Public Library of Science

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7
47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries
47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries
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47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries

Rafique, Munazzah ; AlObaid, Solaiman ; Al‐Jaroudi, Dania

Clinical case reports, 2019-06, Vol.7 (6), p.1238-1241 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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8
The impact of sex chromosome trisomies (XXX, XXY, XYY) on gaze towards faces and affect recognition: a cross-sectional eye tracking study
The impact of sex chromosome trisomies (XXX, XXY, XYY) on gaze towards faces and affect recognition: a cross-sectional eye tracking study
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The impact of sex chromosome trisomies (XXX, XXY, XYY) on gaze towards faces and affect recognition: a cross-sectional eye tracking study

Bouw, Nienke ; Swaab, Hanna ; Tartaglia, Nicole ; Cordeiro, Lisa ; van Rijn, Sophie

Journal of neurodevelopmental disorders, 2022-08, Vol.14 (1), p.44-44, Article 44 [Periódico revisado por pares]

England: BioMed Central Ltd

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9
Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic Woman
Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic Woman
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Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic Woman

Takahashi, Tohru

Internal Medicine, 2014, Vol.53(7), pp.783-787 [Periódico revisado por pares]

Japan: The Japanese Society of Internal Medicine

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10
Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX
Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX
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Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX

Pandelache, Alison ; Francis, David ; Oertel, Ralph ; Dickson, Rebecca ; Sachdev, Rani ; Ling, Ling ; Gamage, Dinusha ; Godler, David E.

Genes, 2021-06, Vol.12 (6), p.798 [Periódico revisado por pares]

Basel: MDPI AG

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