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- A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
- Instability of Short Arm of Acrocentric Chromosomes: Lesson from Non-Acrocentric Satellited Chromosomes
- Novel Genomic Imbalances and Chromosome Translocations Involving C-Myc Gene in Burkitt’S Lymphoma DB Zimonjic, C Keck-Waggoner and NC Popescu
- Is Mitochondrial DNA Depletion Involved in Alzheimer's Disease?
- Synaptonemal Complex Analysis of an X-Autosome Translocation-Carrier in the Domestic Pig Daf Villagomez, M Świtoński, B Singh, Krs Fisher, I Gustavsson, Pk Basrur
- Uniparental Disomy (UPD) Tech Review.Indd
- Extreme Reduction of Chromosome-Specific Α-Satellite Array Is Unusually Common in Human Chromosome 21
- A Case of Partial 14 Trisomy, 47, XX,+Der(14)
- Supplementary Materials and Methods
- Distribution of the D15Z1 Copy Number Polymorphism
- Centromeres Under Pressure: Evolutionary Innovation in Conflict with Conserved Function
- Transcriptome Characterization of Human Mammary Cell Lines Expressing Different Levels of ERBB2 by Serial Analysis of Gene Expression
- Paternal Uniparental Disomy of Chromosome 14 and Unique Exchange of Chromosome 7 in Cases of Spontaneous Abortion
- Methylation Analysis (Of Chromosomes 14 and 15)
- Basic Principles of Human Genetics: a Primer for Oral Medicine Harold C
- Doxorubicin-Induced Translocation of Mtdna Into the Nuclear Genome of Human Lymphocytes Detected Using a Molecular-Cytogenetic Approach
- Supporting Information SI Materials and Methods Mice And
- Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
- Chromosome Changes
- Molecular Analysis of a Chromosomal Translocation, T(9;14)
- Uniparental Propagation of Mitochondrial DNA in Mouse-Human Cell Hybrids
- Exclusion of Maternal Uniparental Disomy of Chromosome 14 In
- E-One Mapping and Medical Genetics
- Brief Clinical Report a Child with Multiple Congenital Anomalies And
- Current Status of Human Chromosome 14 D Kamnasaran,Dwcox
- Reprogramming Pediatric Genetic Disorders: Pearson Syndrome, Ring 14 Syndrome, and Fanconi Anemia
- Integrative Mapping of Gossypium Hirsutum L. by Meiotic Fluorescent in Situ Hybridization of a Tandemly Repetitive Sequence (B77)
- Duplications of 14Q Distal FTNW
- Ring Chromosome 14 Syndrome
- 14 Chromosome Chapter
- Chromosome 14
- Frequent Aneuploidy in Primary Human T Cells Following CRISPR-Cas9 Cleavage
- Supplementary Table 1. a Full List of Cancer Genes
- De Novo Centromere Formation on a Chromosome Fragment in Maize
- Synaptonemal Complex Analysis of an X-Autosome Translocation-Carrier in the Domestic Pig