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- Alternate Centromere Inactivation Ina Pseudodicentric (15;20)(Pter;Pter
- 20Q13.33 Deletions FTNW
- Maternal UPD 20 in a Hyperactive Child with Severe Growth Retardation
- Transcriptome Characterization of Human Mammary Cell Lines Expressing Different Levels of ERBB2 by Serial Analysis of Gene Expression
- 20P Deletions FTNS
- Identification of Potential and Novel Target Genes in Pituitary Prolactinoma by Bioinformatics Analysis
- Chromosome 20 Deletion in Human Multiple Endocrine Neoplasia
- Centromere Detection of Human Metaphase Chromosome Images Using a Candidate Based Method
- Impaired CENP-E Function Renders Large Chromosomes More Vulnerable to Congression Failure
- Uniparental Propagation of Mitochondrial DNA in Mouse-Human Cell Hybrids
- The Complete Sequence of a Human Genome
- Ring Chromosome 20 Syndrome – a Rare Chromosomal Cause of Refractory Epilepsy in Children
- Comprehensive Review on the Molecular Genetics of Autosomal Recessive Primary Cambridge.Org/Grh Microcephaly (MCPH)
- A Partial Short Arm Deletion of Chromosome 20∶
- Wen鄄ting Liao 1,2,3 , Yan Feng 1,2 , Men鄄lin
- Supplementary Table 1: Histopathological Data for Samples Used in Study
- The DNA Sequence and Analysis of Human Chromosome 13
- The Chromosome Shuffle
- REVIEW Neocentromeres: New Insights Into Centromere Structure, Disease Development, and Karyotype Evolution
- Sequence of the Supernumerary B Chromosome of Maize Provides Insight Into Its Drive Mechanism and Evolution
- (12) Patent Application Publication (10) Pub. No.: US 2012/0053062 A1 BROOKS (43) Pub
- Chromosome 20 Containing the Diabetes-Susceptibility
- Ring Chromosome 20 Syndrome Also Known As: R(20) Syndrome, R(20), Ring 20, RC20
- Identification of Potential and Novel Target Genes in Pituitary Prolactinoma by Bioinformatics Analysis
- Duplications of 20P FTNW
- Chromosome 20