Diagnostic testing for uniparental disomy: a points to consider statement from the American College of Medical Genetics and Genomics (ACMG) | Genetics in Medicine
A Systematic Search for Uniparental Disomy in Carriers of Chromosome Translocations | European Journal of Human Genetics
Mandibuloacral Dysplasia Caused by LMNA Mutations and Uniparental Disomy
Maternal Uniparental Disomy of Chromosome 16 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Prader-Willi Syndrome - Pathology Flashcards | Draw it to Know it
New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism in: European Journal of Endocrinology Volume 163 Issue 6 (2010)
Uniparental disomy as a cause of pediatric endocrine disorders. - Abstract - Europe PMC
Uniparental disomy (UPD) formation after the rescue of a trisomic... | Download Scientific Diagram
Clinical significance and mechanisms associated with segmental UPD | Molecular Cytogenetics | Full Text
The Foundation for Prader-Willi Research - PWS is caused by a lack of active genetic material in a particular region of chromosome 15 (15q11-q13). Normally, individuals inherit one copy of chromosome 15
PDF] Uniparental disomy as a cause of pediatric endocrine disorders | Semantic Scholar
Genes | Free Full-Text | Prenatal Detection of Uniparental Disomies (UPD): Intended and Incidental Finding in the Era of Next Generation Genomics