Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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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 |
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2 |
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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3 |
Material Type: Artigo
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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 |
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4 |
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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5 |
Material Type: Artigo
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47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovariesRafique, Munazzah ; AlObaid, Solaiman ; Al‐Jaroudi, DaniaClinical case reports, 2019-06, Vol.7 (6), p.1238-1241 [Periódico revisado por pares]England: John Wiley & Sons, IncTexto completo disponível |
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6 |
Material Type: Artigo
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Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic WomanTakahashi, TohruInternal Medicine, 2014, Vol.53(7), pp.783-787 [Periódico revisado por pares]Japan: The Japanese Society of Internal MedicineTexto completo disponível |
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7 |
Material Type: Artigo
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Patients with 47, XXX karyotype who experienced premature ovarian failure (POF): two case reportsSugawara, Nobuo ; Maeda, Machiko ; Manome, Tomomi ; Nagai, Rie ; Araki, YasuhisaReproductive medicine and biology, 2013-10, Vol.12 (4), p.193-195 [Periódico revisado por pares]Tokyo: Springer JapanTexto completo disponível |
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8 |
Material Type: Artigo
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Molecular Epidemiology of Malaria in Cameroon. XXX. Sequence Analysis of Plasmodium falciparum ATPase 6, Dihydrofolate Reductase, and Dihydropteroate Synthase Resistance Markers in Clinical Isolates from Children Treated with an Artesunate-Sulfadoxine-Pyrimethamine CombinationMENEMEDENGUE, Virginie ; SAHNOUNI, Khalifa ; BASCO, Leonardo ; TAHAR, RachidaThe American journal of tropical medicine and hygiene, 2011-07, Vol.85 (1), p.22-25 [Periódico revisado por pares]Deerfield, IL: American Society of Tropical Medecine and HygieneTexto completo disponível |
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9 |
Material Type: Artigo
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Acromegaly Accompanied by Turner Syndrome with 47,XXX/45,X/46,XX MosaicismYamazaki, Masanori ; Sato, Ai ; Nishio, Shin-ichi ; Takeda, Teiji ; Miyamoto, Takahide ; Katai, Miyuki ; Hashizume, KiyoshiInternal Medicine, 2009, Vol.48(6), pp.447-453 [Periódico revisado por pares]Japan: The Japanese Society of Internal MedicineTexto completo disponível |
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10 |
Material Type: Artigo
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Bienvenidos al XXX Congreso de la Sociedad Española de Medicina Familiar y ComunitariaCampos González, Juan Carlos ; Puig Barberà, JoanAtención primaria, 2010-06, Vol.42 (6), p.305-306 [Periódico revisado por pares]Elsevier EspanaTexto completo disponível |