Pages that link to "Q24604903"
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The following pages link to Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5 (Q24604903):
Displaying 35 items.
- Primary structure of human ribosomal protein S14 and the gene that encodes it (Q24299857) (← links)
- Assignment of the human dihydrofolate reductase gene to the q11----q22 region of chromosome 5 (Q24609496) (← links)
- Human genes involved in cholesterol metabolism: chromosomal mapping of the loci for the low density lipoprotein receptor and 3-hydroxy-3-methylglutaryl-coenzyme A reductase with cDNA probes (Q24610589) (← links)
- Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia (Q24619494) (← links)
- Deletion mapping of human chromosome 5 using chromosome-specific DNA probes (Q24675611) (← links)
- Chromosomal localization of human gene for histidyl-tRNA synthetase: clustering of genes encoding aminoacyl-tRNA synthetases on human chromosome 5 (Q28298683) (← links)
- Determination of the 'critical region' for cat-like cry of Cri-du-chat syndrome and analysis of candidate genes by quantitative PCR (Q28303083) (← links)
- Systematic generation of sequence-tagged sites for physical mapping of human chromosomes: Application to the mapping of human chromosome 7 using yeast artificial chromosomes (Q33326355) (← links)
- Assignment of the human MARS gene, encoding methioninyl-tRNA synthetase, to chromosome 12 using human X Chinese hamster cell hybrids (Q34263952) (← links)
- Isolation and characterization of interspecific heat-resistant hybrids between a temperature-sensitive chinese hamster cell asparaginyl-tRNA synthetase mutant and normal human leukocytes: assignment of human asnS gene to chromosome 18. (Q34271350) (← links)
- Familial 5q11.2----q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia (Q35124129) (← links)
- Molecular analysis of the 18q- syndrome--and correlation with phenotype. (Q35194073) (← links)
- Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5 (Q35197231) (← links)
- Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype (Q35198822) (← links)
- Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus (Q35246016) (← links)
- Comparative map for mice and humans (Q35364327) (← links)
- Mouse chromosome 13. (Q35675737) (← links)
- Chromosomal localization of the human c-fms oncogene (Q35687862) (← links)
- A fine structure physical map of the short arm of chromosome 5 (Q36414854) (← links)
- A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease gene (Q36419339) (← links)
- Overabundance of rare-cutting restriction endonuclease sites in the human genome (Q36426450) (← links)
- Genetic counterselective procedure to isolate interspecific cell hybrids containing single human chromosomes: construction of cell hybrids and recombinant DNA libraries specific for human chromosomes 3 and 4. (Q36458143) (← links)
- A High-Resolution Physical and Transcript Map of the Cri du Chat Region of Human Chromosome 5p (Q36878303) (← links)
- Efficient Procedure for Transferring Specific Human Genes into Chinese Hamster Cell Mutants: Interspecific Transfer of the Human Genes Encoding Leucyl- and Asparaginyl-tRNA Synthetases (Q36938978) (← links)
- Characterization of a Chinese hamster-human hybrid cell line with increased system L amino acid transport activity (Q36942042) (← links)
- Higher eukaryotic aminoacyl-tRNA synthetases in physiologic and pathologic states (Q39746550) (← links)
- A scaffold for the Chinese hamster genome (Q40229524) (← links)
- A rare TaqI RFLP immediately 3' of the HEXB gene on chromosome 5. (Q40448302) (← links)
- Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5. (Q41930144) (← links)
- Assignment of human dihydrofolate reductase gene to band q23 of chromosome 5 and of related pseudogene psi HD1 to chromosome 3. (Q43881222) (← links)
- Mouse chromosome 13. (Q44293939) (← links)
- A Radiation Hybrid Map of Human Chromosome 5 with Integration of Cytogenetic, Genetic, and Transcript Maps (Q46133504) (← links)
- Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase (Q57252359) (← links)
- Comparative map for mice and humans (Q67871559) (← links)
- Gene mapping and linkage analysis in Chinese hamster: Assignment of the genes forAPRT, LDHA, IDH2, andGAA to chromosome 3 (Q70286253) (← links)