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Chromosome 8
Frequent Multiplication of the Long Arm of Chromosome 8 in Hepatocellular Carcinoma1
A Study on Acute Myeloid Leukemias with Trisomy 8, 11, Or 13, Monosomy 7, Or Deletion 5Q
8 Translocation in Burkitt Lymphoma Interrupts the VK Locus (Gene Localization/Immunoglobulin Genes/Genetics of B-Cell Neoplasia/In Situ Hybridization) BEVERLY S
The Cytogenetics of Hematologic Neoplasms 1 5
Rapid Molecular Assays to Study Human Centromere Genomics
Trisomy 8 Mosaicism
Supernumerary Chromosome 8 FTNW
Gene Mapping and Medical Genetics Human Chromosome 8
8P23 Duplication Syndrome
Hypogonadotropic Hypogonadism and Cleft Lip and Palate Caused by A
Human Demography in the Pleistocene: Do Mitochondrial and Nuclear Genes Tell the Same Story?
Human C-Mnc One Gene Is Located on the Region of Chromosome 8
Aneusomies of Chromosomes 8 and Y Detected by Fluorescence in Situ Hybridization Are Prognostic Markers for Pathological Stage C (Pt3nom O) Prostate Carcinoma I
Interruption of Cenph Causes Mitotic Failure and Embryonic Death, And
Human Mitochondrial Topoisomerase I
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Karyotyping and Prenatal Diagnosis of 47,XX,+ 8[67]/46,XX [13]
Novel and Highly Recurrent Chromosomal Alterations in Se´Zary Syndrome
Top View
Chromosome 8 Introduction the Genetic Size of Chromosome 8 Is
8P23 Deletion Syndrome
Origin of Nondisjunction in Trisomy 8 and Trisomy 8 Mosaicism
Extreme Reduction of Chromosome-Specific Α-Satellite Array Is Unusually Common in Human Chromosome 21
Mitochondrial Ribosomal Proteins: Candidate Genes for Mitochondrial Disease James E
Centromere Deletion in Cryptococcus Deuterogattii Leads to Neocentromere Formation and Chromosome Fusions Klaas Schotanus, Joseph Heitman*
Supporting Information SI Materials and Methods Mice And
Partial Trisomy and Monosomy 8P Due to Inversion Duplication
Genomic Characterization of Pleural Solitary Fibrous Tumours
Modifier Locus for Mitochondrial DNA Disease
Chromosome 8
8 Mosaicism As a Possible Mechanism of the Imprinted Birk-Barel Syndrome: a Case Study
Mice Using Multicolor Fluorescence in Situ Hybridization (Aneuploidy/Spermatlds/Sperm/Sex Reversal/Pseudoautosomal Region) TERRY ASHLEY*T, THOMAS RIED**, and DAVID C
Centromere Function and Evolution in Maize (Zea Mays)
Inverted Duplication/Deletion of the Short Arm of Chromosome 8 in Two Patients with Tetralogy of Fallot
Abundant Copy-Number Loss of CYCLOPS and STOP Genes in Gastric Adenocarcinoma
Chromosome 8P Deletions Are Associated with Invasive Tumor Growth in Urinary Bladder Cancer
Humcfs: a Database of Fragile Sites in Human Chromosomes
Comparative Genomic Hybridization Detects Many Recurrent Imbalances
Mining the Gaps of Chromosome 8
REVIEW Neocentromeres: New Insights Into Centromere Structure, Disease Development, and Karyotype Evolution
Genetic Isolation of a Region of Chromosome 8 That Exerts Major Effects on Blood Pressure and Cardiac Mass in the Spontaneously Hypertensive Rat
The Structure, Function, and Evolution of a Complete Human Chromosome 8
Title the Evolutionary Life Cycle of the Resilient Centromere
J Recombinase Mediated Rearrangements in Human Lymphoid