ℹ️
🇬🇧
Search
Search for publications relevant for "Genetic map"
Genetic map
Publication
Class
Person
Publication
Programmes
Export current view
publication
A genetic map of Xenopus tropicalis
2011 |
Faculty of Science
publication
Genetic mapping in the lignin-degrading basidiomycete Phanerochaete chrysosporium
Faculty of Science
publication
Rat hypodactylous mutation-genetic mapping and characterization of congenic strains
Publication without faculty affiliation
publication
Genetic map of AFLP markers in the rat (Rattus norvegicus) derived from the H B/Ipcv and B H/Cub sets of recombinant inbred strains.
2003 |
First Faculty of Medicine
publication
Genetic map of AFLP markers in the rat (Rattus norvegicus) derived from the H B/Ipcv and B H/Cub sets of recombinant inbred strains.
2003 |
Faculty of Physical Education and Sport
publication
Efficient high-throughput sequencing of a laser microdissected chromosome arm
2013 |
Faculty of Science
publication
Derivation of SHR-Chromosome 4 Congenic Sublines for Fine Genetic Mapping of Quantitative Trait Loci with Major Effects on Insulin Resistance and Blood Pressure
2000 |
First Faculty of Medicine
publication
Xenopus Cytogenetics and Chromosomal Evolution
2015 |
Faculty of Science
publication
Heredity
2003 |
Faculty of Science
publication
A novell alloreactivity-controlling locus, Alan1, mapped to mouse chromosome 17
2000 |
Publication without faculty affiliation
publication
A novell alloreactivity-controlling locus, Alan1, mapped to mouse chromosome 17
2000 |
First Faculty of Medicine, Faculty of Mathematics and Physics
publication
Genetic Structure of Europeans: A View from the North-East
2009 |
Second Faculty of Medicine
publication
Data Descriptor: Daphnia magna transcriptome by RNA-Seq across 12 environmental stressors
2016 |
Faculty of Science
publication
A Genome-Wide Analysis of Populations from European Russia Reveals a New Pole of Genetic Diversity in Northern Europe
2013 |
Second Faculty of Medicine
publication
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2
2016 |
First Faculty of Medicine