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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
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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2
Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX
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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3
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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4
VEGF(121)b, a new member of the VEGF(xxx)b family of VEGF-A splice isoforms, inhibits neovascularisation and tumour growth in vivo
VEGF(121)b, a new member of the VEGF(xxx)b family of VEGF-A splice isoforms, inhibits neovascularisation and tumour growth in vivo
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VEGF(121)b, a new member of the VEGF(xxx)b family of VEGF-A splice isoforms, inhibits neovascularisation and tumour growth in vivo

Rennel, E S ; Varey, A H R ; Churchill, A J ; Wheatley, E R ; Stewart, L ; Mather, S ; Bates, D O ; Harper, S J

British journal of cancer, 2009-10, Vol.101 (7), p.1183 [Periódico revisado por pares]

England

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5
Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome
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
Doctors’ experiences of adverse events in secondary care: the professional and personal impact
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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7
The parental origin of the extra X chromosome in 47,XXX females
The parental origin of the extra X chromosome in 47,XXX females
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The parental origin of the extra X chromosome in 47,XXX females

MAY, K. M ; JACOBS, P. A ; LEE, M ; RATCLIFFE, S ; ROBINSON, A ; NIELSEN, J ; HASSOLD, T. J

American journal of human genetics, 1990-04, Vol.46 (4), p.754-761 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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8
The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy
The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy
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The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy

Tartaglia, Nicole ; Howell, Susan ; Wilson, Rebecca ; Janusz, Jennifer ; Boada, Richard ; Martin, Sydney ; Frazier, Jacqueline B ; Pfeiffer, Michelle ; Regan, Karen ; McSwegin, Sarah ; Zeitler, Philip

Journal of multidisciplinary healthcare, 2015, Vol.8 (default), p.323-334 [Periódico revisado por pares]

New Zealand: Dove Medical Press Limited

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9
Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21
Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21
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Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21

Park, V M ; Bravo, R R ; Shulman, L P

Journal of medical genetics, 1995-08, Vol.32 (8), p.650-653 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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10
The evolutionary history of Drosophila buzzatii. XXX. Mitochondrial DNA polymorphism in original and colonizing populations
The evolutionary history of Drosophila buzzatii. XXX. Mitochondrial DNA polymorphism in original and colonizing populations
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The evolutionary history of Drosophila buzzatii. XXX. Mitochondrial DNA polymorphism in original and colonizing populations

Rossi, M S ; Barrio, E ; Latorre, A ; Quezada-Díaz, J E ; Hasson, E ; Moya, A ; Fontdevila, A

Molecular biology and evolution, 1996-02, Vol.13 (2), p.314-323 [Periódico revisado por pares]

United States

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