Clinical significance and mechanisms associated with segmental UPD | Molecular Cytogenetics | Full Text
Diagnostic testing for uniparental disomy: a points to consider statement from the American College of Medical Genetics and Genomics (ACMG) | Genetics in Medicine
OBM Genetics | Uniparental Disomy and Imprinting Disorders
![Box], Disease Example (trisomy rescue) - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK5191/bin/trisomyRescueDiseaseExample.jpg "Box], Disease Example (trisomy rescue) - GeneReviews® - NCBI Bookshelf")
Box], Disease Example (trisomy rescue) - GeneReviews® - NCBI Bookshelf
Hereditary syndrome uniparental disomy (UPD) | Vinmec
Mosaicism and uniparental disomy in prenatal diagnosis: Trends in Molecular Medicine
Genes | Free Full-Text | Prenatal Detection of Uniparental Disomies (UPD): Intended and Incidental Finding in the Era of Next Generation Genomics
Uniparental disomy: Origin, frequency, and clinical significance - Benn - 2021 - Prenatal Diagnosis - Wiley Online Library
Temple syndrome: A patient with maternal hetero-UPD14, mixed iso- and hetero-disomy detected by SNP microarray typing of patient
Uniparental disomy in cancer: Trends in Molecular Medicine
Maternal Uniparental Disomy of Chromosome 16 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Imprinting and Uniparental Disomy for the USMLE Step 1 - YouTube
Maternal Uniparental Disomy of Chromosome 4 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
The Frequency of Uniparental Disomy in Prader-Willi Syndrome — Implications for Molecular Diagnosis | NEJM
New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism in: European Journal of Endocrinology Volume 163 Issue 6 (2010)
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
![Box], Learn More (trisomy rescue) - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK5191/bin/trisomyRescueLearnMore2.jpg "Box], Learn More (trisomy rescue) - GeneReviews® - NCBI Bookshelf")
Box], Learn More (trisomy rescue) - GeneReviews® - NCBI Bookshelf
Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements | Journal of Medical Genetics
Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader–Willi syndrome - ScienceDirect
Prader-Willi Syndrome - Pathology Flashcards | Draw it to Know it
Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome. | Semantic Scholar
Uniparental disomy (UPD) formation after the rescue of a trisomic... | Download Scientific Diagram
Uniparental Disomy and Disorders of Imprinting - Chromosome Abnormalities and Genetic Counseling , 3rd Edition
Uniparental Disomy - an overview | ScienceDirect Topics
![PDF] Uniparental disomy as a cause of pediatric endocrine disorders | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/7ba91b70c7f90db3ec71b707a08bddad5a017231/2-Figure1-1.png "PDF] Uniparental disomy as a cause of pediatric endocrine disorders | Semantic Scholar")
PDF] Uniparental disomy as a cause of pediatric endocrine disorders | Semantic Scholar
Difference Between Mosaicism and Uniparental Disomy | Compare the Difference Between Similar Terms
Genes | Free Full-Text | Prenatal Detection of Uniparental Disomies (UPD): Intended and Incidental Finding in the Era of Next Generation Genomics
