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Chromosome 22
An Overview of the Independent Histories of the Human Y Chromosome and the Human Mitochondrial Chromosome
Organization, Evolution and Function of Alpha Satellite Dna
Basic Genetic Mechanisms— the Ways in Which the Cell Maintains, Replicates, Expresses, and Occasionally Improves the Genetic Information Carried in Its DNA
22Q12 and 22Q13 Duplications
Constitutional 9P22q Translocation in a Patient with Melanoma, Deafness and DNA Repair Deficiency Disrupts P14arf and Down-Regulates TBX1
Chronic Myeloid Leukemia Causes, Risk Factors, and Prevention Risk Factors
Cryptic Subtelomeric Translocations in the 22Q13 Deletion Syndrome J Med Genet: First Published As 10.1136/Jmg.37.1.58 on 1 January 2000
Human Artificial Chromosomes Generated by Modification of a Yeast Artificial Chromosome Containing Both Human Alpha Satellite and Single-Copy DNA Sequences
The Paternal Chromosome 9 and the Maternal Chromosome 22 Are Preferentially Rearranged in Chronic Myeloid Leukaemia
The Genomic Structure of a Human Chromosome 22 Nucleolar Organizer Region Determined by TAR Cloning Jung‑Hyun Kim1,5, Vladimir N
PE2917 22Q11.2 Related Disorders
Chromosome 22 Array-CGH Profiling of Breast Cancer Delimited Minimal Common Regions of Genomic Imbalances and Revealed Frequent Intra-Tumoral Genetic Heterogeneity
Chromosome 22
GENE LIST ANTI-CORRELATED Systematic Common Description
(12) Patent Application Publication (10) Pub. No.: US 2011/0196614 A1 Banchereau Et Al
22 Chromosome Translocation in Chronic Myelocytic Leukemia Detected by Fluorescence in Situ Hybridization
Instability of Short Arm of Acrocentric Chromosomes: Lesson from Non-Acrocentric Satellited Chromosomes
TYMP Gene Thymidine Phosphorylase
Top View
Genetic Signature of Natural Selection in First Americans
6Cognitive and Behavioral Characteristics of Children With
Molecular Genetic Analysis of Chromosome 22 in 81 Cases of Meningioma1
Uman Enome News
Digeorge Syndrome Critical Region of Human Chromosome 22 St~Phanie Lorain, 1 Suzanne Demczuk, 2 Val~Rie Lamour, 1 Steve Toth, 3 Alain Aurias, 2 Bruce A
Abnormal Chromosome 22 and Recurrence of Trisomy-22 Syndrome* BEVERLY S
Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
Fetal Loss: a Genetic Insight of the De Novo Accessory Bi-Satellited
Research Progress of Chimeric RNA and Health
Evidence for an Ependymoma Tumour Suppressor Gene In
22Q11.2 Deletion Syndrome
The Complete Sequence of a Human Genome
What Can the Y Chromosome Tell Us About the Origin of Modern Humans?
Ring 22 FTNW
On Chromosome 22 (Brain Tumors/Neurofibromatosis/Recessive Oncogenes/DNA Markers/Inherited Disease Genes) BERND R
The Organisation of Repetitive Sequences in the Pericentromeric Region of Human Chromosome 10
22Q11.2 Distal Deletion Syndrome
Derivative Chromosome 9 Deletions Are a Significant Feature Of
High Resolution Chromosome 3P, 8P, 9Q and 22Q Allelotyping Analysis in the Pathogenesis of Gallbladder Carcinoma
Percept Is Different
Consequences of 22Q11.2 Microdeletion on the Genome, Individual and Population Levels
Breakpoints on Chromosomes 9 and 22 in Philadelphia Chromosome-Positive Chronic Myelogenous Leukemia (CML)
Humcfs: a Database of Fragile Sites in Human Chromosomes
22 Chromosome Chapter
Chimeras Taking Shape: Potential Functions of Proteins Encoded by Chimeric RNA Transcripts
Comparative Genomic Hybridization Detects Many Recurrent Imbalances
Coexistence of Autism and Ring Chromosome 22
B-Binding Sites Across Human Chromosome 22
Supplementary Table 1. a Full List of Cancer Genes
Chimeras Taking Shape: Potential Functions of Proteins Encoded by Chimeric RNA Transcripts