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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
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
How Much More XXX is Generation X Consuming? Evidence of Changing Attitudes and Behaviors Related to Pornography Since 1973
How Much More XXX is Generation X Consuming? Evidence of Changing Attitudes and Behaviors Related to Pornography Since 1973
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How Much More XXX is Generation X Consuming? Evidence of Changing Attitudes and Behaviors Related to Pornography Since 1973

Price, Joseph ; Patterson, Rich ; Regnerus, Mark ; Walley, Jacob

The Journal of sex research, 2016-01, Vol.53 (1), p.12-20 [Periódico revisado por pares]

United States: Taylor & Francis

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3
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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4
A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome
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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5
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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6
A Spontaneous Pregnancy in a Patient with Turner Syndrome with 45,X/47,XXX Mosaicism: A Case Report and Review of the Literature
A Spontaneous Pregnancy in a Patient with Turner Syndrome with 45,X/47,XXX Mosaicism: A Case Report and Review of the Literature
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A Spontaneous Pregnancy in a Patient with Turner Syndrome with 45,X/47,XXX Mosaicism: A Case Report and Review of the Literature

Mavridi, Artemis ; Ntali, Georgia ; Theodora, Marianna ; Stamatelopoulos, Kimon ; Michala, Lina

Journal of pediatric & adolescent gynecology, 2018-12, Vol.31 (6), p.651-654 [Periódico revisado por pares]

United States: Elsevier Inc

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7
Generation of integration-free induced pluripotent stem cells (GZHMUi001-A) by reprogramming peripheral blood mononuclear cells from a 47, XXX syndrome patient
Generation of integration-free induced pluripotent stem cells (GZHMUi001-A) by reprogramming peripheral blood mononuclear cells from a 47, XXX syndrome patient
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Generation of integration-free induced pluripotent stem cells (GZHMUi001-A) by reprogramming peripheral blood mononuclear cells from a 47, XXX syndrome patient

Chen, Yuchang ; Ou, Zhanhui ; Song, Bing ; Xian, Yexing ; Ouyang, Shuming ; Xie, Yuhuan ; Xue, Yanting ; Sun, Xiaofang

Stem cell research, 2017-08, Vol.23 (C), p.57-60 [Periódico revisado por pares]

England: Elsevier B.V

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8
47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal development
47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal development
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47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal development

Brambila-Tapia, Aniel Jessica Leticia, M.D., M.Sc ; Rivera, Horacio, M.D., Ph.D ; García-Castillo, Herbert, M.D., M.Sc ; Domínguez-Quezada, Maria Guadalupe, Ph.D ; Dávalos-Rodríguez, Ingrid Patricia, M.D., Ph.D

Fertility and sterility, 2009-11, Vol.92 (5), p.1747.e5-1747.e7 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis
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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10
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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