Chromosome 16
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- 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