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- Implication of Chromosome 11 in the Suppression of Neoplastic Expression in Human Cell Hybrids1
- A Comprehensive Genetic Map of Murine Chromosome 11 Reveals Extensive Linkage Conservation Between Mouse and Human
- Molecular Cytogenetic Analysis of 10;11 Rearrangements in Acute
- Somatic Loss of Maternal Chromosome 11 Causes Parent-Of-Origin-Dependent Inheritance in SDHD-Linked Paraganglioma and Phaeochromocytoma Families
- Centromeres Under Pressure: Evolutionary Innovation in Conflict with Conserved Function
- Centromeres of Human Chromosomes
- Birth, Evolution, and Transmission of Satellite-Free Mammalian Centromeric Domains
- Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
- Centromere Repeats: Hidden Gems of the Genome
- Allele Loss on Chromosome 10 and Point Mutation of Ras Oncogenes Are Infrequent in Tumors of MEN 2 A
- This Is a Test
- Case Report Application of Microarray-Based Comparative Genomic Hybridization in Prenatal and Postnatal Settings: Three Case Reports
- Identification of Two Independent X-Autosome Translocations in Closely Related Mammalian (Proechimys) Species
- Gain of 11Q by an Additional Ring Chromosome 11 and Trisomy 18 in CD5-Positive Intravascular Large B-Cell Lymphoma
- Late Replication in an X-Autosome Translocation in the Mouse
- Allelic Loss from Chromosome 11 in Parathyroid Tumors
- Supplementary Data for Classification, Subtype
- Dynamic Turnover of Centromeres Drives Karyotype Evolution in Drosophila Ryan Bracewell, Kamalakar Chatla, Matthew J Nalley, Doris Bachtrog*
- Complex Karyotype Including Ring Chromosome 11 in a Patient with Acute Myeloid Leukemia: Case Report
- Uniparental Propagation of Mitochondrial DNA in Mouse-Human Cell Hybrids
- Interstitial Deletion of the Long Arm of Chromosome 11 Determined by Fluorescence in Situ Hybridization
- Familial Pericentric Inversion of Chromosome 11 Detected Prenatally .Da
- Asynchronous Replication of Alleles in Genomes Carrying an Extra Autosome
- Cytogenetics: Nomenclature and Disease
- Regional Assignment of 68 New Human Gene Transcripts on Chromosome 11
- Analysis of the Functional Role of Chromosome 10 Loss in Human Glioblastomas1
- X-Chromosome Inactivation
- Chromosome Analysis: Banding Patterns and Structural Aberrations David F
- English, Dutch, German, French, Spanish, Italian and Danish 11Q Research and Resource Group Medical Advisor Paul Grossfeld, MDI [email protected]
- Human Chromosome 11 Contains Two Different Growth Suppressor Genes for Embryonal Rhabdomyosarcoma
- The Insulin Gene Is Located on the Short Arm of Chromosome 11 in Humans DAVID OWERBACH, GRAEME I
- Humcfs: a Database of Fragile Sites in Human Chromosomes
- Trisomy 11 in Myelodysplastic Syndromes Defines a Unique Group of Disease with Aggressive Clinicopathologic Features
- A Novel Multiple FISH Array for the Detection of Genetic Aberrations in Cancer
- 11;22 Translocation FTNW
- Supplementary Table 1. a Full List of Cancer Genes
- Title the Evolutionary Life Cycle of the Resilient Centromere
- Selective Loss of Chromosome 11 in Pheochromocytomas Associated with the VHL Syndrome
- Diatom Centromeres Suggest a Mechanism for Nuclear DNA
- Evolutionary History of Chromosome 11 Featuring Four Distinct Centromere Repositioning Events in Catarrhini