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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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2
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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3
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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4
The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination
The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination
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The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination

MacDonald, M. ; Hassold, T. ; Harvey, J. ; Wang, L.H. ; Morton, N.E. ; Jacobs, P.

Human molecular genetics, 1994-08, Vol.3 (8), p.1365-1371 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
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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6
Comparing Sex Steroid Levels During the Annual Cycles of Rainbow Trout (Oncorhynchus mykiss) Diploid Female (XX) and Triploid Female (XXX) Genotypic Sex
Comparing Sex Steroid Levels During the Annual Cycles of Rainbow Trout (Oncorhynchus mykiss) Diploid Female (XX) and Triploid Female (XXX) Genotypic Sex
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Comparing Sex Steroid Levels During the Annual Cycles of Rainbow Trout (Oncorhynchus mykiss) Diploid Female (XX) and Triploid Female (XXX) Genotypic Sex

Espinosa, E ; Josa, A ; Gil, L ; Malo, C ; Mitjana, O

Reproduction in domestic animals, 2013-02, Vol.48 (1), p.149-155 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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7
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation
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Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation

Chen, Chih-Ping, M.D ; Lin, Shuan-Pei, M.D ; Tsai, Fuu-Jen, M.D ; Chern, Schu-Rern, MS ; Wang, Wayseen, MS

Fertility and sterility, 2008-06, Vol.89 (6), p.1826.e5-1826.e7 [Periódico revisado por pares]

United States: Elsevier Inc

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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
Duodenal atresia in an infant with triple‐X syndrome: A new associated malformation in 47,XXX
Duodenal atresia in an infant with triple‐X syndrome: A new associated malformation in 47,XXX
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Duodenal atresia in an infant with triple‐X syndrome: A new associated malformation in 47,XXX

Rolle, Udo ; Linse, Barbara ; Glasow, Simone ; Sandig, Klaus Rainer ; Richter, Thomas ; Till, Holger

Birth defects research. A Clinical and molecular teratology, 2007-08, Vol.79 (8), p.612-613 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
Turner syndrome and 45,X/47,XXX mosaicism
Turner syndrome and 45,X/47,XXX mosaicism
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Turner syndrome and 45,X/47,XXX mosaicism

Akbas, E ; Mutluhan, H ; Savasoglu, K ; Soylemez, F ; Ozturk, I ; Yazici, G

Genetic counseling, 2009-01, Vol.20 (2), p.141 [Periódico revisado por pares]

Switzerland

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