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1 |
Material Type: Artigo
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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 |
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2 |
Material Type: Artigo
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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 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 |
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3 |
Material Type: Artigo
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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 studyBouw, Nienke ; Swaab, Hanna ; Tartaglia, Nicole ; Cordeiro, Lisa ; van Rijn, SophieJournal of neurodevelopmental disorders, 2022-08, Vol.14 (1), p.44-44, Article 44 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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4 |
Material Type: Artigo
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VEGF₁₂₁b and VEGF₁₆₅b are weakly angiogenic isoforms of VEGF-ACatena, Raúl ; Larzabal, Leyre ; Larrayoz, Marta ; Molina, Eva ; Hermida, Jose ; Agorreta, Jackeline ; Montes, Ramon ; Pio, Ruben ; Montuenga, Luis M ; Calvo, AlfonsoMolecular cancer, 2010-12, Vol.9 (319), p.320-320, Article 320 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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5 |
Material Type: Artigo
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Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experienceMargiotti, Katia ; Cesta, Anthony ; Dello Russo, Claudio ; Cima, Antonella ; Barone, Maria Antonietta ; Viola, Antonella ; Sparacino, Davide ; Mesoraca, Alvaro ; Giorlandino, ClaudioBMC research notes, 2020-03, Vol.13 (1), p.167-167, Article 167 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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6 |
Material Type: Artigo
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Molecular evolutionary and structural analysis of familial exudative vitreoretinopathy associated FZD4 geneSeemab, Suman ; Pervaiz, Nashaiman ; Zehra, Rabail ; Anwar, Saneela ; Bao, Yiming ; Abbasi, Amir AliBMC ecology and evolution, 2019-03, Vol.19 (1), p.72-72, Article 72 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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7 |
Material Type: Artigo
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Evidence-based recommendations for delivering the diagnosis of X & Y chromosome multisomies in children, adolescents, and young adults: an integrative reviewRiggan, Kirsten A ; Ormond, Kelly E ; Allyse, Megan A ; Close, SharronBMC pediatrics, 2024-04, Vol.24 (1), p.263-263, Article 263 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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8 |
Material Type: Artigo
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A patient with Turner syndrome received the percutaneous vertebroplasty seven times: a case report and literature reviewLi, Longyu ; Shi, Yifang ; Zhao, Nan ; Liu, Zhengpei ; Zhao, Zhe ; Song, Zongmian ; Zheng, Sailei ; Yan, Miaoheng ; Leng, Zikuan ; Chen, Songfeng ; Shang, Guowei ; Kou, Hongwei ; Liu, HongjianEuropean journal of medical research, 2021-12, Vol.26 (1), p.139-139, Article 139 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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9 |
Material Type: Artigo
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Does the birth plan match what is relevant to women? Preferences of Spanish women when giving birthArtieta-Pinedo, Isabel ; Paz-Pascual, Carmen ; Garcia-Alvarez, Arturo ; Bully, Paola ; Espinosa, MaiteBMC women's health, 2024-01, Vol.24 (1), p.42-12, Article 42 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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10 |
Material Type: Artigo
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Autism spectrum disorder associated with 49,XYYYY: case report and review of the literatureDemily, Caroline ; Poisson, Alice ; Peyroux, Elodie ; Gatellier, Valérie ; Nicolas, Alain ; Rigard, Caroline ; Schluth-Bolard, Caroline ; Sanlaville, Damien ; Rossi, MassimilianoBMC medical genetics, 2017-01, Vol.18 (1), p.9-9, Article 9 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |