Search Results (59)

MatchTypeWhy
Chromosome MappingConcept Why?
Physical Chromosome MappingConcept Why?
Developmental Dysplasia of the Hip: Linkage Mapping and Whole Exome Sequencing Identify a Shared Variant in CX3CR1 in All Affected Members of a Large Multigeneration Family.Academic Article Why?
Linkage Mapping and Whole Exome Sequencing Identify a Shared Variant in CX3CR1 in a Large Multi-Generation Family.Academic Article Why?
A detailed physical map of the 6p reading disability locus, including new markers and confirmation of recombination suppression.Academic Article Why?
Chromosome locations of the MYB related genes, AMYB and BMYB.Academic Article Why?
Genomic approaches to DNA repair and mutagenesis.Academic Article Why?
Location of the 9257 and ataxia mutations on mouse chromosome 18.Academic Article Why?
MicroRNA genes are frequently located near mouse cancer susceptibility loci.Academic Article Why?
Rabbit calcium-sensing receptor (CASR) gene: chromosome location and evidence for related genes.Academic Article Why?
Recombination mapping of the susceptibility region for sporadic inclusion body myositis within the major histocompatibility complex.Academic Article Why?
The nature and identification of quantitative trait loci: a community's view.Academic Article Why?
TOM: enhancement and extension of a tool suite for in silico approaches to multigenic hereditary disorders.Academic Article Why?
Vahidnezhad, HassanPerson Why?
Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15.Academic Article Why?
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