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- Distribution of the D15Z1 Copy Number Polymorphism
- The Prader-Willi Syndrome and Interstitial Deletion of Chromosome 15
- Handbook on Genetics
- Illustrations Depicting Chromosome 15 and the UBE3A Gene
- Basic Principles of Human Genetics: a Primer for Oral Medicine Harold C
- Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
- Prader-Willi Syndrome
- Uniparental Propagation of Mitochondrial DNA in Mouse-Human Cell Hybrids
- Tetrasomy 15Q26: a Distinct Syndrome Or Shprintzen-Goldberg Syndrome Phenocopy?
- Chromosome 15 Structural Abnormalities: Effect on IGF1R Gene Expression and Function
- 15Q13.3 Microdeletion
- Rare Autosomal Trisomy & NIPT
- Chromosome 15 in Floppy Infants Copyright
- 15Q Deletions FTNW
- ISOCHROMOSOME NEOCENTROMERE 15Qter MOSAICISM Siri Huston, Yvette Rush, Tom Hempel, Ann Olney, Hope Chipman and Warren G
- Supplemental Table 1
- Genome-Wide Linkage Analysis of Gene Expression of Loin Muscle Tissue Identifies Candidate Genes in Pigs
- Supernumerary Marker of Chromosome 15 Associated With
- Humcfs: a Database of Fragile Sites in Human Chromosomes
- Chromosome 15
- What Is a Centromere?
- Neurodevelopmental Disorders Associated with Chromosome 15
- Variant Complex Translocations Involving Chromosomes 1, 9, 9, 15
- Supplementary Table 1. a Full List of Cancer Genes
- The Association of Angelman's Syndrome with Deletions Within 15Qll-13
- Angelman Syndrome, and Uniparental Disomy Resulting from Paternal Meiosis II Non-Disjunction S Roberts, F Maggouta, R Thompson, S Price, S Thomas
- 15Q11-Q13 Duplication Syndrome
- RCH FRACP Genetics 2005 Complex Genetic Mechanisms