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Chromosome 16
Human Chromosome‐Specific Aneuploidy Is Influenced by DNA
Searching the Genomes of Inbred Mouse Strains for Incompatibilities That Reproductively Isolate Their Wild Relatives
16P11.2 Deletion Syndrome Guidebook
Definition of the Landscape of Promoter DNA Hypomethylation in Liver Cancer
How Genes Work
Gene Mapping and Medical Genetics
Rapid Molecular Assays to Study Human Centromere Genomics
Comparative Mapping of DNA Markers from the Familial Alzheimer Mouse Chromosomes 16 and 17
16 Chromosome Chapter
1 SUPPLEMENTARY RESULTS Hypomethylated Promoters Are
Quantitative Trait Loci Mapping of Macrophage Atherogenic Phenotypes
The Mapping of Chromosome 16
Receptor Signaling Through Osteoclast-Associated Monocyte
Duplications of 16P FTNW
The Mapping of Chromosome 16
Supplementary Table 3. Genes Specifically Regulated by Zol (Non-Significant for Fluva)
Physical Mapping of Human Chromosome 16
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Top View
Genetic Linkage Map of 46 DNA Markers on Human Chromosome 16
Extreme Reduction of Chromosome-Specific Α-Satellite Array Is Unusually Common in Human Chromosome 21
16P13.11 Microduplications FTNW.Pdf
WHAT's DIFFERENT ABOUT CHROMOSOME 16? Raymond
Construction of a Map of Chromosome 16 by Using Radiation Hybrids (Somatic Cell Hybrids/Physical Maps/Multiple Pairwise Analysis) I
Handbook on Genetics
Transcriptome Characterization of Human Mammary Cell Lines Expressing Different Levels of ERBB2 by Serial Analysis of Gene Expression
Paternal Uniparental Disomy of Chromosome 14 and Unique Exchange of Chromosome 7 in Cases of Spontaneous Abortion
Supporting Information SI Materials and Methods Mice And
Familial Translocation T(9;16)
Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
Case Report Application of Microarray-Based Comparative Genomic Hybridization in Prenatal and Postnatal Settings: Three Case Reports
Constitutional Chromosome 16Q Mosaicism: Inheritance and Phenotypic Effects 16
16P12.2 Microdeletion
Changes in Chromosome 16 Firmly Linked to Autism
Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome In
16Q Deletions FTNW
An Analysis of Common Isodisomic Regions in Five Mupd 16 Probands
TK2 Gene Thymidine Kinase 2, Mitochondrial
Partial Trisomy 16 As a Result of Familial 16;20 Translocation
9Q34 & 16P13 Chromosome Duplications in Autism
REVIEW Neocentromeres: New Insights Into Centromere Structure, Disease Development, and Karyotype Evolution
Studies of Fragile Sites on Human Chromosome 16
Cytogenetics
Chromosome 16
Uniparental Propagation of Mitochondrial DNA in Mouse
16P11.2 Microdeletions