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11
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
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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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

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12
47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries
47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries
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47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries

Rafique, Munazzah ; AlObaid, Solaiman ; Al‐Jaroudi, Dania

Clinical case reports, 2019-06, Vol.7 (6), p.1238-1241 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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13
The impact of sex chromosome trisomies (XXX, XXY, XYY) on gaze towards faces and affect recognition: a cross-sectional eye tracking study
The impact of sex chromosome trisomies (XXX, XXY, XYY) on gaze towards faces and affect recognition: a cross-sectional eye tracking study
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The impact of sex chromosome trisomies (XXX, XXY, XYY) on gaze towards faces and affect recognition: a cross-sectional eye tracking study

Bouw, Nienke ; Swaab, Hanna ; Tartaglia, Nicole ; Cordeiro, Lisa ; van Rijn, Sophie

Journal of neurodevelopmental disorders, 2022-08, Vol.14 (1), p.44-44, Article 44 [Periódico revisado por pares]

England: BioMed Central Ltd

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14
Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX
Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX
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Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX

Pandelache, Alison ; Francis, David ; Oertel, Ralph ; Dickson, Rebecca ; Sachdev, Rani ; Ling, Ling ; Gamage, Dinusha ; Godler, David E.

Genes, 2021-06, Vol.12 (6), p.798 [Periódico revisado por pares]

Basel: MDPI AG

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15
Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literature
Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literature
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Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literature

Tang, Ruiyi ; Lin, Lin ; Guo, Zaixin ; Hou, Haiyan ; Yu, Qi

Molecular genetics & genomic medicine, 2019-07, Vol.7 (7), p.e00732-n/a [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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16
Double trisomy (XXX+21 karyotype) in a six-year-old girl with down phenotype
Double trisomy (XXX+21 karyotype) in a six-year-old girl with down phenotype
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Double trisomy (XXX+21 karyotype) in a six-year-old girl with down phenotype

Vergara-Mendez, Laura Daniela ; Talero-Gutiérrez, Claudia ; Velez-Van-Meerbeke, Alberto

Journal of genetics, 2018-03, Vol.97 (1), p.337-340 [Periódico revisado por pares]

New Delhi: Springer India

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17
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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18
Placental Histomorphology in a Case of Double Trisomy 48,XXX,+18
Placental Histomorphology in a Case of Double Trisomy 48,XXX,+18
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Placental Histomorphology in a Case of Double Trisomy 48,XXX,+18

Shah, Sujal I. ; Dyer, Lisa ; Stanek, Jerzy Kulka, Janina

Case reports in pathology, 2018-01, Vol.2018, p.2839765-5 [Periódico revisado por pares]

United States: Hindawi

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19
45,X/47,XXX Mosaicism and Short Stature
45,X/47,XXX Mosaicism and Short Stature
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45,X/47,XXX Mosaicism and Short Stature

Everest, Erica ; Tsilianidis, Laurie A. ; Haider, Anzar ; Rogers, Douglas G. ; Raissouni, Nouhad ; Schweiger, Bahareh Cogulu, Ozgur

Case reports in pediatrics, 2015-01, Vol.2015, p.263253-3 [Periódico revisado por pares]

United States: Hindawi Publishing Corporation

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20
What history tells us XXX. The emergence of the fluid mosaic model of membranes
What history tells us XXX. The emergence of the fluid mosaic model of membranes
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What history tells us XXX. The emergence of the fluid mosaic model of membranes

Morange, Michel

Journal of biosciences, 2013-03, Vol.38 (1), p.3-7 [Periódico revisado por pares]

India: Springer-Verlag

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