Prenatal diagnosis of paternal uniparental disomy for chromosome 14 using a single-nucleotide-polymorphism-based microarray analysis: A case report

Keyphrases

• Microarray Analysis 100%
• Single nucleotide Polymorphism 100%
• Chromosome 14 100%
• Prenatal Diagnosis 100%
• Paternal Uniparental Disomy 100%
• Uniparental Disomy 100%
• Affymetrix 66%
• Clinical Features 33%
• Loss of Heterozygosity 33%
• Fetus 33%
• Thoracic Wall 33%
• Postmortem Examination 33%
• Aborted Fetuses 33%
• Week of Gestation 33%
• Normal Karyotype 33%
• Craniofacial Abnormalities 33%
• Maternal Uniparental Disomy 14 33%
• Imprinting Disorders 33%
• Ultrasound Features 33%
• Abnormal Ultrasound 33%
• Abdominal Wall Defect 33%

Medicine and Dentistry

• Microarray Analysis 100%
• Single Nucleotide Polymorphism 100%
• Prenatal Diagnosis 100%
• Uniparental Disomy 100%
• Chromosome 14 100%
• Clinical Feature 20%
• Heterozygosity 20%
• Pregnancy 20%
• Karyotype 20%
• Autopsy 20%
• Abdominal Wall Defect 20%
• Chest Wall 20%
• Uridine Diphosphate 20%
• Fetus Death 20%
• Craniofacial Malformation 20%
• Diseases 20%

Biochemistry, Genetics and Molecular Biology

• Single-Nucleotide Polymorphism 100%
• Chromosome 14 100%
• Uniparental Disomy 100%
• Loss of Heterozygosity 20%
• Uridine Diphosphate 20%
• Karyotype 20%
• Pregnancy 20%