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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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2
The comorbidity landscape of 47,XXX syndrome: A nationwide epidemiologic study
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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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 of non-mosaic X trisomy (65,XXX) in a Thoroughbred mare confirmed by cytogenetic and molecular analysis
A case of non-mosaic X trisomy (65,XXX) in a Thoroughbred mare confirmed by cytogenetic and molecular analysis
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A case of non-mosaic X trisomy (65,XXX) in a Thoroughbred mare confirmed by cytogenetic and molecular analysis

Cieslak, Jakub ; Mackowski, Mariusz ; Skrzetuska, Weronika ; Fidos-Tama, Ewa ; Siwinska, Natalia ; Szczerbal, Izabela

Journal of applied genetics, 2024-05, Vol.65 (2), p.395-398 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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5
Double trisomy 48,XXX,+18 with multiple dysmorphic features
Double trisomy 48,XXX,+18 with multiple dysmorphic features
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Double trisomy 48,XXX,+18 with multiple dysmorphic features

Jiang, Zi-Yan ; Wu, Xiao-Hui ; Zou, Chao-Chun

World journal of pediatrics : WJP, 2015-02, Vol.11 (1), p.83-88 [Periódico revisado por pares]

Heidelberg: Childrens Hospital, Zhejiang University School of Medicine

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6
Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)
Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)
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Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)

Xu, Gefeng ; Huang, Tianqing ; Jin, Xian ; Cui, Cunhe ; Li, Depeng ; Sun, Cong ; Han, Ying ; Mu, Zhenbo

Fish physiology and biochemistry, 2016-02, Vol.42 (1), p.193-202 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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7
Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetus
Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetus
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Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetus

Gabriele, Tonni ; Gianpaolo, Grisolia

Archives of gynecology and obstetrics, 2013-07, Vol.288 (1), p.3-11 [Periódico revisado por pares]

Berlin/Heidelberg: Springer-Verlag

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8
Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, India
Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, India
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Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, India

Balwan, Wahied Khawar ; Kumar, Parvinder ; Raina, T. R. ; Gupta, Subash

Journal of genetics, 2008-12, Vol.87 (3), p.257-259 [Periódico revisado por pares]

India: Springer-Verlag

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9
Crohn's disease in Turner's syndrome with X-chromosomal mosaicism of 45 XO and 47 XXX
Crohn's disease in Turner's syndrome with X-chromosomal mosaicism of 45 XO and 47 XXX
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Crohn's disease in Turner's syndrome with X-chromosomal mosaicism of 45 XO and 47 XXX

Ohkawara, Tatsuya ; Takeda, Hiroshi ; Miyashita, Kencho ; Kato, Mototsugu ; Asaka, Masahiro ; Sugiyama, Toshiro ; Nishihira, Jun

Journal of gastroenterology, 2005-09, Vol.40 (9), p.914-916 [Periódico revisado por pares]

Japan: Springer Nature B.V

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10
Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX
Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX
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Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX

Reish, Orit ; Berryman, Todd ; Cunningham, Thomas R ; Sher, Carron ; Oetting, William S

Chromosome research, 2004-01, Vol.12 (2), p.125-132 [Periódico revisado por pares]

Netherlands: Springer Nature B.V

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