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 Syndrome Gene Urinary tract infection Ultrasound Stillbirth Monosomy Magnetic resonance imaging Genetic counseling Chromosome Chromosomal translocation Trisomy Protein Obesity Hypertension Phenotype DNA Polymerase chain reaction Messenger RNA Acid Prostate Pneumonia Sepsis Escherichia coli Sonication X-ray crystallography Scanning electron microscope Logistic regression Gestational age Odds ratio Disease Karyotype CT scan Nuclear magnetic resonance Medical ultrasound Biopsy Ovarian cancer Breast cancer Genome Single-nucleotide polymorphism
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Publications tagged with this subject: 14

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1. Knockdown of Myo-Inositol Transporter SMIT1 Normalizes Cholinergic and Glutamatergic Function in an Immortalized Cell Line Established from the Cerebral Cortex of a Trisomy 16 Fetal Mouse, an Animal Model of Human Trisomy 21 (Down Syndrome)

2. Genome-wide gene expression analysis in the placenta from fetus with trisomy 21

3. Incompatible with Care: Examining Trisomy 18 Medical Discourse and Families’ Counter-discourse for Recuperative Ethos

4. Prenatal congenital vertical talus (rocker bottom foot): a marker for multisystem anomalies

5. Factors Influencing Outcomes After Cardiac Intervention in Infants with Trisomy 13 and 18

6. Differential Brain, Cognitive and Motor Profiles Associated with Partial Trisomy. Modeling Down Syndrome in Mice

7. Women’s Experience with Non-Invasive Prenatal Testing and Emotional Well-being and Satisfaction after Test-Results

8. Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction

9. Transient Fanconi syndrome in two preterm infants with hydronephrosis and urinary tract infection

10. Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations

11. Principles of first trimester screening in the age of non-invasive prenatal diagnosis: screening for chromosomal abnormalities

12. Chromosome 21-Encoded microRNAs (mRNAs): Impact on Down’s Syndrome and Trisomy-21 Linked Disease

13. Molecular cytogenetic characterisation of a novel de novo ring chromosome 6 involving a terminal 6p deletion and terminal 6q duplication in the different arms of the same chromosome

14. Non-invasive prenatal testing (NIPT): Europe’s first multicenter post-market clinical follow-up study validating the quality in clinical routine


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