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1
The comorbidity landscape of 47,XXX syndrome: A nationwide epidemiologic study
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The comorbidity landscape of 47,XXX syndrome: A nationwide epidemiologic study

Berglund, Agnethe ; Stochholm, Kirstine ; Gravholt, Claus Højbjerg

Genetics in medicine, 2022-02, Vol.24 (2), p.475-487 [Periódico revisado por pares]

United States: Elsevier Inc

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2
Resting-state functional connectivity in adults with 47,XXX: a 7 Tesla MRI study
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Resting-state functional connectivity in adults with 47,XXX: a 7 Tesla MRI study

Serrarens, Chaira ; Kashyap, Sriranga ; Riveiro-Lago, Laura ; Otter, Maarten ; Campforts, Bea C M ; Stumpel, Constance T R M ; Jansma, Henk ; Linden, David E J ; van Amelsvoort, Thérèse A M J ; Vingerhoets, Claudia

Cerebral cortex (New York, N.Y. 1991), 2023-04, Vol.33 (9), p.5210-5217 [Periódico revisado por pares]

United States: Oxford University Press

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3
Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory
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Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory

Petersen, Andrea K. ; Cheung, Sau Wai ; Smith, Janice L. ; Bi, Weimin ; Ward, Patricia A. ; Peacock, Sandra ; Braxton, Alicia ; Van Den Veyver, Ignatia B. ; Breman, Amy M.

American journal of obstetrics and gynecology, 2017-12, Vol.217 (6), p.691.e1-691.e6 [Periódico revisado por pares]

United States: Elsevier Inc

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4
伴有生长迟缓的47,XXX综合征3例报道
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伴有生长迟缓的47,XXX综合征3例报道

杨利 ; 冯亚琴 ; 杨玉 ; 谢理玲 ; 王荻兰 ; 黄慧

上海交通大学学报(医学版), 2021-11, Vol.41 (11), p.1425-1428

南昌大学附属儿童医院/江西省儿童医院内分泌遗传代谢科,南昌330006

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5
The epidemiology of sex chromosome abnormalities
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Artigo
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The epidemiology of sex chromosome abnormalities

Berglund, Agnethe ; Stochholm, Kirstine ; Gravholt, Claus Højbjerg

American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.202-215

Hoboken, USA: John Wiley & Sons, Inc

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6
45,X/46,XX at the first amniocentesis, and 45,X/47,XXX/46,XX at the repeat amniocentesis and at birth in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the 45,X cell line and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes
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Artigo
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45,X/46,XX at the first amniocentesis, and 45,X/47,XXX/46,XX at the repeat amniocentesis and at birth in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the 45,X cell line and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes

Chen, Chih-Ping ; Wu, Fang-Tzu ; Pan, Yen-Ting ; Wu, Peih-Shan ; Chen, Wen-Lin ; Lee, Meng-Shan ; Wang, Wayseen

Taiwanese journal of obstetrics & gynecology, 2023-11, Vol.62 (6), p.901-905 [Periódico revisado por pares]

Elsevier B.V

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7
Perinatal detection of disomy X cell line by fluorescence in situ hybridization in a pregnancy with 45,X/47,XXX at amniocentesis, cytogenetic discrepancy in various tissues and a favorable outcome
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Perinatal detection of disomy X cell line by fluorescence in situ hybridization in a pregnancy with 45,X/47,XXX at amniocentesis, cytogenetic discrepancy in various tissues and a favorable outcome

Chen, Chih-Ping ; Wu, Fang-Tzu ; Pan, Yen-Ting ; Wu, Peih-Shan ; Chen, Wen-Lin ; Lee, Meng-Shan ; Wang, Wayseen

Taiwanese journal of obstetrics & gynecology, 2023-11, Vol.62 (6), p.906-909 [Periódico revisado por pares]

Elsevier B.V

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8
Incidence of sex chromosome aneuploidy in a prenatal population: 27‐year longitudinal study in Northern Italy
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Incidence of sex chromosome aneuploidy in a prenatal population: 27‐year longitudinal study in Northern Italy

Samango‐Sprouse, C. A. ; Grati, F. R. ; Brooks, M. ; Hamzik, M. P. ; Khaksari, K. ; Gropman, A. ; Taylor, A. ; Malvestiti, F. ; Grimi, B. ; Liuti, R. ; Milani, S. ; Chinetti, S. ; Trotta, A. ; Agrati, C. ; Repetti, E. ; Martin, K. A.

Ultrasound in obstetrics & gynecology, 2023-08, Vol.62 (2), p.266-272 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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9
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
Triple X supergirls: Their special educational needs and social experience
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Triple X supergirls: Their special educational needs and social experience

Attfield, Kate

International journal of educational research, 2020, Vol.102, p.101588, Article 101588 [Periódico revisado por pares]

Elsevier Ltd

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