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Chromosome 5
The Human Gene Encoding Phosphatidylinositol-3 Kinase Associated P85a Is at Chromosome Region 5Ql2-13'
Cytogenetic and Molecular Delineation of the Smallest Commonly Deleted Region of Chromosome 5 in Malignant Myeloid Diseases
The Cytogenetics of Hematologic Neoplasms 1 5
Cri-Du-Chat Syndrome Diagnosed in a 21-Year-Old Woman by Means of Comparative Genomic Hybridization
Allele-Specific Disparity in Breast Cancer Fatemeh Kaveh1, Hege Edvardsen1, Anne-Lise Børresen-Dale1,2, Vessela N Kristensen1,2,3* and Hiroko K Solvang1,4
Human Chromosome-Specific Cdna Libraries: New Tools for Gene Identification and Genome Annotation
5Q14.3 Deletions FTNW
Deletions and Losses in Chromosomes 5 Or 7 in Adult Acute
Rare Allelic Forms of PRDM9 Associated with Childhood Leukemogenesis
Ring Chromosome 5 with Dental Anomalies
The Human Gene Encoding Phosphatidylinositol-3 Kinase Associated P85a Is at Chromosome Region 5Ql2-13'
Gain of Chromosome 4Qter and Loss of 5Pter: an Unusual Case with Features of Cri Du Chat Syndrome
The Chicken Genome Has a Hybrid Centromere Model, Involving Either Long Arrays of Tandem Repeats on Some Chromosomes Or Relative
Receptor Signaling Through Osteoclast-Associated Monocyte
The Interleukin 3 Gene Is Located on Human Chromosome 5 and Is Deleted in Myeloid Leukemias with a Deletion of 5Q
GENE LIST ANTI-CORRELATED Systematic Common Description
Mitochondrial Pseudogenes Suggest Repeated Inter-Species Hybridization in Hominid Evolution
Mapping Chromosome 5
Top View
Trisomy 5P Inverted Duplication & Deletion of 5Pftnp
Centromere-Mediated Chromosome Break Drives Karyotype Evolution in Closely Related 2 Malassezia Species
Inherited 5P Deletion Syndrome Due to Paternal Balanced Translocation: Phenotypic Heterogeneity Due to Duplication of 8Q and 12P
NDUFS6 Mutations Are a Novel Cause of Lethal Neonatal Mitochondrial Complex I Deficiency
Chromosome 5
Chromosome 5 Introduction the Size of Chromosome 5 (180 Mb) and The
Trisomy 5P: Duplications of 5P15
Genetics and Mitochondrial Abnormalities in Autism Spectrum Disorders: a Review
Centromere Deletion in Cryptococcus Deuterogattii Leads to Neocentromere Formation and Chromosome Fusions Klaas Schotanus, Joseph Heitman*
Condensin I Associates with Structural and Gene Regulatory Regions in Vertebrate Chromosomes
HHS Public Access Author Manuscript
Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
Centromere Repeats: Hidden Gems of the Genome
Gene Mapping and Medical Genetics Genetic Markers on Chromosome 7
Nuclear-Mitochondrial DNA Segments Resemble Paternally Inherited Mitochondrial DNA in Humans
Cancer-Associated Alteration of Pericentromeric Heterochromatin May Contribute to Chromosome Instability
Location of the Centromeres on the Linkage Maps of Maize'
Centromere Scission Drives Chromosome Shuffling and Reproductive Isolation
Basic Human Genetics: Reproductive Health and Chromosome Abnormalities
And CENP-E Kinesins Biol
X-Chromosome Inactivation
Centromere Scission Drives Chromosome Shuffling and Reproductive Isolation
Genetic Abnormalities and Pathophysiology of MDS
Humcfs: a Database of Fragile Sites in Human Chromosomes