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Match	Type	Why
Identification and applications of repetitive probes for gene mapping in the mouse.	Academic Article	Why?
Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19.	Academic Article	Why?
Chromosome Mapping	Concept	Why?
Physical Chromosome Mapping	Concept	Why?
Assignment of microrchidia (Morc) to mouse chromosome 16 by interspecific backcross linkage analysis and human chromosome 3q13 using somatic cell hybrids and in situ hybridization.	Academic Article	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?
[Cloning of the gene leg-arista-wing complex and analysis of its mutant derivatives in Drosophila].	Academic Article	Why?
A detailed physical map of the 6p reading disability locus, including new markers and confirmation of recombination suppression.	Academic Article	Why?
A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36.	Academic Article	Why?
A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcross.	Academic Article	Why?
A high-resolution linkage map of the lethal spotting locus: a mouse model for Hirschsprung disease.	Academic Article	Why?
A high-resolution linkage map of the tight skin 2 (Tsk2) locus: a mouse model for scleroderma (SSc) and other cutaneous fibrotic diseases.	Academic Article	Why?
A homozygous deletion within the carbonic anhydrase-like domain of the Ptprg gene in murine L-cells.	Academic Article	Why?
A molecular genetic linkage map of mouse chromosome 2.	Academic Article	Why?

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