58 results on '"uniparental disomy"'
Search Results
2. Ring Chromosome 7
3. Laboratory Testing for Prader-Willi Syndrome
4. Placental Mesenchymal Dysplasia
5. Hereditary Overgrowth Syndromes
6. Hepatoblastoma Family of Tumors: Risk Factors and Pathogenic Pathways
7. Developmental Delay: Gene Testing
8. Epigenetic Control of Genome Expression
9. Introduction
10. Prenatal Cytogenetic and Cytogenomic Diagnosis
11. The Role of Genetics and Epigenetics in Growth Restriction
12. Preimplantation Diagnosis for Chromosomal Disorders
13. Beckwith–Wiedemann Syndrome
14. Prader–Willi Syndrome
15. Angelman Syndrome
16. I(1p), I(1q) Syndrome
17. Imprinting Disorders of Early Childhood
18. Centric Small Supernumerary Marker Chromosomes
19. Microarrays, Postnatal Analysis, and Implications for Growth Monitoring
20. Molecular Changes in Myelodysplastic Syndrome
21. Prenatal Diagnosis and Genetic Counseling
22. Angelman Syndrome
23. Chromosomal Deletions in AML
24. Epigenetics
25. Imprinted Genes and Human Disease: An Evolutionary Perspective
26. Prenatal Diagnosis
27. Wilms Tumor (nephroblastoma)
28. Developmental Disabilities
29. inv dup(15) and inv dup(22)
30. Laboratory Testing for Prader-Willi Syndrome
31. Pyknodysostosis
32. Preimplantation Genetic Diagnosis for Chromosomal Disorders
33. Genomic Imprinting and Uniparental Disomy
34. Autosomal Aneuploidy
35. Human Chromosome Nomenclature : An Overview and Definition of Terms
36. Abortion and the Placenta in Chromosomal Anomalies
37. Genetic Inheritance
38. Chorion Villus Sampling in the First Trimester
39. Neonatal Diabetes
40. Euploid Chromosome Aberrations, Uniparental Disomy, and Genomic Imprinting
41. Effect of Embryo Culture on Imprinted Gene Expression in the Preimplantation Mouse Embryo
42. Kinship and Genomic Imprinting
43. Genomic Imprinting: Its Role in Development and Disease
44. Prader-Willi and Angelman Syndromes
45. An Overview of Molecular Genetics
46. Interference, Heterogeneity and Disease Gene Mapping
47. Parental Imprinting in Mammalian Development
48. Numerically Abnormal Chromosome Constitutions in Humans
49. Current Understanding and Recurrence Risks of Prader-Willi and Angelman Syndromes
50. Clinical Findings in Individuals with Angelman Syndrome without a Molecular Deletion or Uniparental Disomy
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