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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
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study
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Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study

Gruchy, Nicolas ; Blondeel, Eleonore ; Le Meur, Nathalie ; Joly-Hélas, Géraldine ; Chambon, Pascal ; Till, Marianne ; Herbaux, Martine ; Vigouroux-Castera, Adeline ; Coussement, Aurélie ; Lespinasse, James ; Amblard, Florence ; Jimenez Pocquet, Mélanie ; Lebel-Roy, Camille ; Carré-Pigeon, Frédérique ; Flori, Elisabeth ; Mugneret, Francine ; Jaillard, Sylvie ; Yardin, Catherine ; Harbuz, Radu ; Collonge-Rame, Marie-Agnès ; Vago, Philippe ; Valduga, Mylène ; Leporrier, Nathalie ; Vialard, François

Prenatal diagnosis, 2016-06, Vol.36 (6), p.523-529 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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3
Attention-Deficit Hyperactivity Disorder Symptoms in Children and Adolescents with Sex Chromosome Aneuploidy: XXY, XXX, XYY, and XXYY
Attention-Deficit Hyperactivity Disorder Symptoms in Children and Adolescents with Sex Chromosome Aneuploidy: XXY, XXX, XYY, and XXYY
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Attention-Deficit Hyperactivity Disorder Symptoms in Children and Adolescents with Sex Chromosome Aneuploidy: XXY, XXX, XYY, and XXYY

TARTAGLIA, Nicole R ; AYARI, Natalie ; HUTAFF-LEE, Christa ; BOADA, Richard

Journal of developmental and behavioral pediatrics, 2012-05, Vol.33 (4), p.309-318 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events
Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events
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Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events

Szalai, A. J. ; Alarcón, G. S. ; Calvo-Alén, J. ; Toloza, S. M. A. ; McCrory, M. A. ; Edberg, J. C. ; McGwin, G. ; Bastian, H. M. ; Fessler, B. J. ; Vilá, L. M. ; Kimberly, R. P. ; Reveille, J. D.

Rheumatology (Oxford, England), 2005-07, Vol.44 (7), p.864-868 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes
Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes
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Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes

Patwardhan, Anil J. ; Brown, Wendy E. ; Bender, Bruce G. ; Linden, Mary G. ; Eliez, Stephan ; Reiss, Allan L.

American journal of medical genetics, 2002-01, Vol.114 (1), p.93-98 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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Root length in the permanent teeth of women with an additional X chromosome (47,XXX females)
Root length in the permanent teeth of women with an additional X chromosome (47,XXX females)
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Root length in the permanent teeth of women with an additional X chromosome (47,XXX females)

Lähdesmäki, Raija E. ; Alvesalo, Lassi J.

Acta odontologica Scandinavica, 2010-07, Vol.68 (4), p.223-227 [Periódico revisado por pares]

England: Taylor & Francis

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7
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
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Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18

Chen, Chih‐Ping ; Chern, Schu‐Rern ; Yeh, Li‐Fan ; Chen, Wen‐Lin ; Chen, Li‐Feng ; Wang, Wayseen

Prenatal diagnosis, 2000-09, Vol.20 (9), p.750-753 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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8
Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second Trimester
Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second Trimester
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Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second Trimester

Fernández-Moya, J.M. ; Sanz, R. ; Rodríguez de Alba, M. ; Ibañez, M.A. ; Ayuso, C. ; Díaz-Recasens, J. ; Robledo, M. ; Ramos, C.

Fetal diagnosis and therapy, 2000-03, Vol.15 (2), p.97-101 [Periódico revisado por pares]

Basel, Switzerland: Karger

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9
Divergent phenotypes among 48,XXXX and 47,XXX females
Divergent phenotypes among 48,XXXX and 47,XXX females
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Divergent phenotypes among 48,XXXX and 47,XXX females

Telfer, M A ; Richardson, C E ; Helmken, J ; Smith, G F

American journal of human genetics, 1970-05, Vol.22 (3), p.326-335 [Periódico revisado por pares]

United States

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10
A psychiatric-cytogenetic study of a female patient with 45-46-47 chromosomes and sex chromosomoes XO-XX-XXX
A psychiatric-cytogenetic study of a female patient with 45-46-47 chromosomes and sex chromosomoes XO-XX-XXX
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A psychiatric-cytogenetic study of a female patient with 45-46-47 chromosomes and sex chromosomoes XO-XX-XXX

Nielsen, J ; Thomsen, N

Acta psychiatrica Scandinavica, 1968, Vol.44 (2), p.141-155 [Periódico revisado por pares]

United States

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