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Expanding the phenotype of mosaic trisomy 20 - Willis - 2008 - American Journal of Medical Genetics Part A - Wiley Online Library
![Children | Free Full-Text | Additional Evidence for Neuropsychiatric Manifestations in Mosaic Trisomy 20: A Case Report and Brief Review Children | Free Full-Text | Additional Evidence for Neuropsychiatric Manifestations in Mosaic Trisomy 20: A Case Report and Brief Review](https://pub.mdpi-res.com/children/children-08-01030/article_deploy/html/images/children-08-01030-g001.png?1637717179)
Children | Free Full-Text | Additional Evidence for Neuropsychiatric Manifestations in Mosaic Trisomy 20: A Case Report and Brief Review
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Trisomy First, Translocation Second, Uniparental Disomy and Partial Trisomy Third: A New Mechanism for Complex Chromosomal Aneuploidy | European Journal of Human Genetics
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Mosaic trisomies. (A) Mosaic trisomy 9 (20%) in patient no. 17, with no... | Download Scientific Diagram
![Pure trisomy 20p resulting from isochromosome formation and whole arm translocation | Journal of Medical Genetics Pure trisomy 20p resulting from isochromosome formation and whole arm translocation | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/37/6/454/F1.large.jpg?width=800&height=600&carousel=1)
Pure trisomy 20p resulting from isochromosome formation and whole arm translocation | Journal of Medical Genetics
![Diagnostics | Free Full-Text | De Novo Mosaic 6p23-p25.3 Tetrasomy Caused by a Small Supernumerary Marker Chromosome Presenting Trisomy Distal 6p Phenotype: A Case Report and Literature Review Diagnostics | Free Full-Text | De Novo Mosaic 6p23-p25.3 Tetrasomy Caused by a Small Supernumerary Marker Chromosome Presenting Trisomy Distal 6p Phenotype: A Case Report and Literature Review](https://www.mdpi.com/diagnostics/diagnostics-12-02306/article_deploy/html/images/diagnostics-12-02306-g001-550.jpg)
Diagnostics | Free Full-Text | De Novo Mosaic 6p23-p25.3 Tetrasomy Caused by a Small Supernumerary Marker Chromosome Presenting Trisomy Distal 6p Phenotype: A Case Report and Literature Review
![PDF) Uniparental disomy and the phenotype of mosaic trisomy 20: A new case and review of the literature PDF) Uniparental disomy and the phenotype of mosaic trisomy 20: A new case and review of the literature](https://i1.rgstatic.net/publication/26701625_Uniparental_disomy_and_the_phenotype_of_mosaic_trisomy_20_A_new_case_and_review_of_the_literature/links/55b77b7a08ae092e965717f6/largepreview.png)
PDF) Uniparental disomy and the phenotype of mosaic trisomy 20: A new case and review of the literature
![Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome - ScienceDirect Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1028455920300267-gr1.jpg)
Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome - ScienceDirect
![A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14) | Human Genome Variation A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14) | Human Genome Variation](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41439-020-00113-x/MediaObjects/41439_2020_113_Fig1_HTML.jpg)
A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14) | Human Genome Variation
Friends of Serenity - The most common Trisomy 20 is mosaic Trisomy 20. Approximately 90-95% of babies with Trisomy 20 survive prenatally. Common characteristics of children born with Trisomy 20 include spinal
![PDF) Additional Evidence for Neuropsychiatric Manifestations in Mosaic Trisomy 20: A Case Report and Brief Review PDF) Additional Evidence for Neuropsychiatric Manifestations in Mosaic Trisomy 20: A Case Report and Brief Review](https://i1.rgstatic.net/publication/356120668_Additional_Evidence_for_Neuropsychiatric_Manifestations_in_Mosaic_Trisomy_20_A_Case_Report_and_Brief_Review/links/61a239ceacc0bc46c11b2f0c/largepreview.png)
PDF) Additional Evidence for Neuropsychiatric Manifestations in Mosaic Trisomy 20: A Case Report and Brief Review
![Low‐level mosaicism of trisomy 14: Phenotypic and molecular characterization - Shinawi - 2008 - American Journal of Medical Genetics Part A - Wiley Online Library Low‐level mosaicism of trisomy 14: Phenotypic and molecular characterization - Shinawi - 2008 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/9b431b69-77a7-4a08-ba23-b8fceb924333/mfig005.jpg)
Low‐level mosaicism of trisomy 14: Phenotypic and molecular characterization - Shinawi - 2008 - American Journal of Medical Genetics Part A - Wiley Online Library
![Pure trisomy 20p resulting from isochromosome formation and whole arm translocation | Journal of Medical Genetics Pure trisomy 20p resulting from isochromosome formation and whole arm translocation | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/37/6/454/F2.large.jpg?width=800&height=600&carousel=1)
Pure trisomy 20p resulting from isochromosome formation and whole arm translocation | Journal of Medical Genetics
![Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure | Genetics in Medicine Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure | Genetics in Medicine](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fgim.2015.103/MediaObjects/41436_2016_Article_BFgim2015103_Fig1_HTML.jpg)
Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure | Genetics in Medicine
![Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies - Ensenauer - 2005 - American Journal of Medical Genetics Part A - Wiley Online Library Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies - Ensenauer - 2005 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/5484d9f7-e406-439b-9c8d-ca4ec2133c6c/mfig002.jpg)