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Refinado por: Base de dados/Biblioteca: Journals@Ovid Complete remover xxx: xxx remover Open Access: PubMed Central remover
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1
Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case report
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Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case report

Liang, Dong ; Han, Minmin ; Xu, Linxin ; Ren, Yi ; Zhang, Yi ; Yin, Jianhong ; Yang, Jing ; Liu, Yunfeng

Medicine (Baltimore), 2022-10, Vol.101 (43), p.e31443-e31443 [Periódico revisado por pares]

United States: Lippincott Williams & Wilkins

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2
A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome
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A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome

Lenroot, 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 Ltd

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3
Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX
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Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX

van Rijn, S. ; Swaab, H.

Genes, brain and behavior, 2015-02, Vol.14 (2), p.200-208 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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4
Differential Expression of VEGF-A xxx Isoforms Is Critical for Development of Pulmonary Fibrosis
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Differential Expression of VEGF-A xxx Isoforms Is Critical for Development of Pulmonary Fibrosis

Barratt, Shaney L ; Blythe, Thomas ; Jarrett, Caroline ; Ourradi, Khadija ; Shelley-Fraser, Golda ; Day, Michael J ; Qiu, Yan ; Harper, Steve ; Maher, Toby M ; Oltean, Sebastian ; Hames, Thomas J ; Scotton, Chris J ; Welsh, Gavin I ; Bates, David O ; Millar, Ann B

American journal of respiratory and critical care medicine, 2017-08, Vol.196 (4), p.479-493 [Periódico revisado por pares]

United States

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5
Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome
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Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome

Sybert, V P

Journal of medical genetics, 2002-03, Vol.39 (3), p.217-221 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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6
Preparation and fabrication of a full‐scale, sagittal‐sliced, 3D‐printed, patient‐specific radiotherapy phantom
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Preparation and fabrication of a full‐scale, sagittal‐sliced, 3D‐printed, patient‐specific radiotherapy phantom

Craft, Daniel F. ; Howell, Rebecca M.

Journal of applied clinical medical physics, 2017-09, Vol.18 (5), p.285-292 [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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7
Doctors’ experiences of adverse events in secondary care: the professional and personal impact
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Doctors’ experiences of adverse events in secondary care: the professional and personal impact

Harrison, Reema ; Lawton, Rebecca ; Stewart, Kevin

Clinical medicine (London, England), 2014-12, Vol.14 (6), p.585-590 [Periódico revisado por pares]

London: Elsevier Ltd

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8
Assessment of PlanIQ Feasibility DVH for head and neck treatment planning
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Assessment of PlanIQ Feasibility DVH for head and neck treatment planning

Fried, David V. ; Chera, Bhishamjit S. ; Das, Shiva K.

Journal of applied clinical medical physics, 2017-09, Vol.18 (5), p.245-250 [Periódico revisado por pares]

United States: John Wiley and Sons Inc

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9
Prenatal diagnosis of fetal hydrops associated with Down's syndrome in a 40‐year‐old woman with a mosaic Turner's karyotype (45,X/47,XXX)
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Prenatal diagnosis of fetal hydrops associated with Down's syndrome in a 40‐year‐old woman with a mosaic Turner's karyotype (45,X/47,XXX)

Acharya, Ganesh ; Jonsrud, Chistoffer ; Van Der Hagen, CarlBirger ; Maltau, Jan Martin

Acta obstetricia et gynecologica Scandinavica, 2003-08, Vol.82 (8), p.773-774 [Periódico revisado por pares]

Oxford, UK: Munksgaard International Publishers

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10
Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidy
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Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidy

Müller, U ; Weber, J L ; Berry, P ; Kupke, K G

Journal of medical genetics, 1993-07, Vol.30 (7), p.597-600 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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