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Material Type: Artigo
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Early symptoms of autism spectrum disorder (ASD) in 1–8 year old children with sex chromosome trisomies (XXX, XXY, XYY), and the predictive value of joint attentionBouw, Nienke ; Swaab, Hanna ; Tartaglia, Nicole ; Wilson, Rebecca L. ; Van der velde, Kim ; van Rijn, SophieEuropean child & adolescent psychiatry, 2023-11, Vol.32 (11), p.2323-2334 [Periódico revisado por pares]Berlin/Heidelberg: Springer Berlin HeidelbergTexto completo disponível |
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Material Type: Artigo
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Double trisomy 48,XXX,+18 with multiple dysmorphic featuresJiang, Zi-Yan ; Wu, Xiao-Hui ; Zou, Chao-ChunWorld journal of pediatrics : WJP, 2015-02, Vol.11 (1), p.83-88 [Periódico revisado por pares]Heidelberg: Childrens Hospital, Zhejiang University School of MedicineTexto completo disponível |
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Material Type: Artigo
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Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)Xu, Gefeng ; Huang, Tianqing ; Jin, Xian ; Cui, Cunhe ; Li, Depeng ; Sun, Cong ; Han, Ying ; Mu, ZhenboFish physiology and biochemistry, 2016-02, Vol.42 (1), p.193-202 [Periódico revisado por pares]Dordrecht: Springer NetherlandsTexto completo disponível |
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Material Type: Artigo
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Double trisomy (XXX+21 karyotype) in a six-year-old girl with down phenotypeVergara-Mendez, Laura Daniela ; Talero-Gutiérrez, Claudia ; Velez-Van-Meerbeke, AlbertoJournal of genetics, 2018-03, Vol.97 (1), p.337-340 [Periódico revisado por pares]New Delhi: Springer IndiaTexto completo disponível |
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Material Type: Artigo
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Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetusGabriele, Tonni ; Gianpaolo, GrisoliaArchives of gynecology and obstetrics, 2013-07, Vol.288 (1), p.3-11 [Periódico revisado por pares]Berlin/Heidelberg: Springer-VerlagTexto completo disponível |
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Material Type: Artigo
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Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, IndiaBalwan, Wahied Khawar ; Kumar, Parvinder ; Raina, T. R. ; Gupta, SubashJournal of genetics, 2008-12, Vol.87 (3), p.257-259 [Periódico revisado por pares]India: Springer-VerlagTexto completo disponível |
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Material Type: Artigo
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Crohn's disease in Turner's syndrome with X-chromosomal mosaicism of 45 XO and 47 XXXOhkawara, Tatsuya ; Takeda, Hiroshi ; Miyashita, Kencho ; Kato, Mototsugu ; Asaka, Masahiro ; Sugiyama, Toshiro ; Nishihira, JunJournal of gastroenterology, 2005-09, Vol.40 (9), p.914-916 [Periódico revisado por pares]Japan: Springer Nature B.VTexto completo disponível |
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Material Type: Artigo
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The ancient claudin Dni2 facilitates yeast cell fusion by compartmentalizing Dni1 into a membrane subdomainCurto, M.-Ángeles ; Moro, Sandra ; Yanguas, Francisco ; Gutiérrez-González, Carmen ; Valdivieso, M.-HenarCellular and molecular life sciences : CMLS, 2018-05, Vol.75 (9), p.1687-1706 [Periódico revisado por pares]Cham: Springer International PublishingTexto completo disponível |
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Material Type: Artigo
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Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXXReish, Orit ; Berryman, Todd ; Cunningham, Thomas R ; Sher, Carron ; Oetting, William SChromosome research, 2004-01, Vol.12 (2), p.125-132 [Periódico revisado por pares]Netherlands: Springer Nature B.VTexto completo disponível |
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Material Type: Artigo
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47,XXX females, sex chromosomes, and tooth crown structureAlvesalo, L ; Tammisalo, E ; Therman, EHuman genetics, 1987-12, Vol.77 (4), p.345-348 [Periódico revisado por pares]GermanyTexto completo disponível |