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1
The behavioral profile of children aged 1–5 years with sex chromosome trisomy (47,XXX, 47,XXY, 47,XYY)
The behavioral profile of children aged 1–5 years with sex chromosome trisomy (47,XXX, 47,XXY, 47,XYY)
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The behavioral profile of children aged 1–5 years with sex chromosome trisomy (47,XXX, 47,XXY, 47,XYY)

Urbanus, Evelien ; Swaab, Hanna ; Tartaglia, Nicole ; Cordeiro, Lisa ; Rijn, Sophie

American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.444-455

Hoboken, USA: John Wiley & Sons, Inc

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2
Early impact of X‐ and Y‐chromosome variations (XXX, XXY, XYY) on social communication and social emotional development in 1–2‐year‐old children
Early impact of X‐ and Y‐chromosome variations (XXX, XXY, XYY) on social communication and social emotional development in 1–2‐year‐old children
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Early impact of X‐ and Y‐chromosome variations (XXX, XXY, XYY) on social communication and social emotional development in 1–2‐year‐old children

Bouw, Nienke ; Swaab, Hanna ; Tartaglia, Nicole ; Jansen, Anna C. ; Rijn, Sophie

American journal of medical genetics. Part A, 2022-07, Vol.188 (7), p.1943-1953 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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3
Epigenetic and transcriptomic consequences of excess X‐chromosome material in 47,XXX syndrome—A comparison with Turner syndrome and 46,XX females
Epigenetic and transcriptomic consequences of excess X‐chromosome material in 47,XXX syndrome—A comparison with Turner syndrome and 46,XX females
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Epigenetic and transcriptomic consequences of excess X‐chromosome material in 47,XXX syndrome—A comparison with Turner syndrome and 46,XX females

Nielsen, Morten Muhlig ; Trolle, Christian ; Vang, Søren ; Hornshøj, Henrik ; Skakkebæk, Anne ; Hedegaard, Jakob ; Nordentoft, Iver ; Pedersen, Jakob Skou ; Gravholt, Claus Højbjerg

American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.279-293

Hoboken, USA: John Wiley & Sons, Inc

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4
A review of trisomy X (47,XXX)
A review of trisomy X (47,XXX)
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A review of trisomy X (47,XXX)

Tartaglia, Nicole R ; Howell, Susan ; Sutherland, Ashley ; Wilson, Rebecca ; Wilson, Lennie

Orphanet journal of rare diseases, 2010-05, Vol.5 (1), p.8-8, Article 8 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
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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6
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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7
Incidence, puberty, and fertility in 45,X/47,XXX mosaicism: Report of a patient and a literature review
Incidence, puberty, and fertility in 45,X/47,XXX mosaicism: Report of a patient and a literature review
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Incidence, puberty, and fertility in 45,X/47,XXX mosaicism: Report of a patient and a literature review

Lim, Han Hyuk ; Kil, Hong Ryang ; Koo, Sun Hoe

American journal of medical genetics. Part A, 2017-07, Vol.173 (7), p.1961-1964 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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8
Double Autosomal/Gonosomal Mosaic Trisomy 47,XXX/47,XX,+14 in a Newborn with Multiple Congenital Anomalies
Double Autosomal/Gonosomal Mosaic Trisomy 47,XXX/47,XX,+14 in a Newborn with Multiple Congenital Anomalies
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Double Autosomal/Gonosomal Mosaic Trisomy 47,XXX/47,XX,+14 in a Newborn with Multiple Congenital Anomalies

Massara, Lucía S. ; Delea, Marisol ; Espeche, Lucía ; Bruque, Carlos D. ; Oliveri, Jaen ; Brun, Paloma ; Furforo, Lilian ; Dain, Liliana ; Rozental, Sandra

Cytogenetic and genome research, 2019-01, Vol.159 (3), p.137-142 [Periódico revisado por pares]

Basel, Switzerland

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9
Incidence, puberty, and fertility in 45,X/47,XXX mosaicism: Report of a patient and a literature review
Incidence, puberty, and fertility in 45,X/47,XXX mosaicism: Report of a patient and a literature review
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Incidence, puberty, and fertility in 45,X/47,XXX mosaicism: Report of a patient and a literature review

Martin, Richard J. ; Smith, Geoff ; Hughes, James ; Morrison, Patrick J.

American journal of medical genetics. Part A, 2018-04, Vol.176 (4), p.1029-1029 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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10
Mortality and incidence in women with 47,XXX and variants
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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