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1
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
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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3
Poor socio-economic status in 47,XXX – An unexpected effect of an extra X chromosome
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Poor socio-economic status in 47,XXX – An unexpected effect of an extra X chromosome

Stochholm, Kirstine ; Juul, Svend ; Gravholt, Claus H

European journal of medical genetics, 2013-06, Vol.56 (6), p.286-291 [Periódico revisado por pares]

Netherlands: Elsevier Masson SAS

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4
Mortality and incidence in women with 47,XXX and variants
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Mortality and incidence in women with 47,XXX and variants

Stochholm, Kirstine ; Juul, Svend ; Gravholt, Claus Højbjerg

American journal of medical genetics. Part A, 2010-02, Vol.152A (2), p.367-372 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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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
Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis
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Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis

Wigby, Kristen ; D'Epagnier, Cheryl ; Howell, Susan ; Reicks, Amy ; Wilson, Rebecca ; Cordeiro, Lisa ; Tartaglia, Nicole

American journal of medical genetics. Part A, 2016-11, Vol.170A (11), p.2870-2881 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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7
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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8
Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: Implications for prenatal counseling and estrogen therapy at puberty
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Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: Implications for prenatal counseling and estrogen therapy at puberty

Blair, Joanne ; Tolmie, John ; Hollman, Anne S. ; Donaldson, Malcolm D.C.

The Journal of pediatrics, 2001-11, Vol.139 (5), p.724-728 [Periódico revisado por pares]

New York, NY: Mosby, Inc

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9
Sports-related maxillofacial fractures: A retrospective study of 125 patients
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Sports-related maxillofacial fractures: A retrospective study of 125 patients

Mourouzis, C. ; Koumoura, F.

International journal of oral and maxillofacial surgery, 2005-09, Vol.34 (6), p.635-638 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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10
Triple X syndrome with rare phenotypic presentation
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Triple X syndrome with rare phenotypic presentation

Jagadeesh, Sujatha ; Jabeen, Gazala ; Bhat, Lathaa ; Vasikarla, Madhavi ; Suresh, Arvind ; Seshadri, Suresh ; Lata, S.

Indian journal of pediatrics, 2008-06, Vol.75 (6), p.629-631 [Periódico revisado por pares]

India: Springer-Verlag

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