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Trisomy

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Neonatal cytogenetic validation demonstrates high accuracy of single-nucleotide polymorphism-based non-invasive prenatal testing: a 4466-case single-center study.
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Sex-specific developmental phenotypes and their response to neonatal <i>Dyrk1a</i> reduction in the Ts65Dn Down syndrome mouse model
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Gain of heterozygosity: an embryo-only, single-nucleotide polymorphism-based method to identify meiotic trisomies in preimplantation genetic testing for aneuploidy.
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Mutational Landscape and Clinical Outcomes in AML With Sole Trisomy 8.
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Genetic and Clinical Characteristics of Chromosome 15q11-q13 Duplication Syndrome in Chinese Children.
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Excess EEG beta-band oscillations in Dup15q syndrome correlate with clinical severity.
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Identification of chromosomal abnormalities in miscarriages using single-nucleotide polymorphism arrays.
Trisomy
Natural History of Prenatally Identified Children with 48,XXYY Syndrome in Infancy and Early Childhood
Trisomy
Early Developmental Sequelae and Neurobiological Phenotype of Patient With 1q24.2q44 Trisomy.
Trisomy
LONG-TERM NEURODEVELOPMENTAL AND COGNITIVE OUTCOMES FOLLOWING PRENATAL INHIBITION OF DYRK1A BY LEUCETTINE L41 IN MOUSE MODELS OF DOWN SYNDROME
Trisomy

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