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1 using fluorescent in situ hybridization and radiation hybrid mapping.
2 on human chromosome 11q25, as determined by radiation hybrid mapping.
3 human chromosome 5q (near the centromere) by radiation hybrid mapping.
4 and between markers D15S209 and AFM321ZD5 by radiation hybrid mapping.
5 both fluorescence in situ hybridization and radiation hybrid mapping.
6 ificial chromosome (YAC) pool screening, and radiation hybrid mapping.
7 ce in situ hybridization, YAC screening, and radiation hybrid mapping.
8 23 regions, respectively, by cytogenetic and radiation hybrid mapping.
9 d integrated with the current genetic map by radiation hybrid mapping.
10 ed by fluorescence in situ hybridization and radiation hybrid mapping.
11 RD was localized to human chromosome 3q27 by radiation hybrid mapping.
12 tu hybridization and is linked to D10S603 by radiation hybrid mapping.
13 a was excluded from this disease interval by radiation hybrid mapping.
14 arrowest disease interval by STS content and radiation hybrid mapping.
15 the gene on chromosome 2q by high resolution radiation hybrid mapping.
17 mapped this gene to human chromosome 4q22 by radiation hybrid mapping and by hybridization to two ove
19 locks, we analyzed 148 markers on CFA9 using radiation hybrid mapping and established a four-way comp
21 ion of selected STSs and bacterial clones by radiation hybrid mapping and fluorescence in situ hybrid
22 length human enamelin cDNA and determined by radiation hybrid mapping and fluorescent in situ hybridi
24 somal localization of Optc was determined by radiation hybrid mapping and its genomic structure deter
26 ntiation Complex (EDC) at chromosome 1q21 by radiation hybrid mapping and STS content of genomic clon
29 hairless, was localized in this interval by radiation hybrid mapping, and a missense mutation was fo
33 approach that is analogous to linkage or to radiation hybrid mapping, but that circumvents many of t
34 the interval between D16S510 and D16S509 by radiation hybrid mapping, corresponding to chromosomal b
46 g DNA loci that exploits many advantages of 'radiation hybrid' mapping in taxa for which such hybrids
51 rmed to originate from BAC 78138 at 19q13.3; radiation hybrid mapping localized EHD3 and EHD4 to 2p21
61 is supported by phylogenetic analysis and by radiation hybrid mapping of murine I-TAC (gene symbol Sc
63 nalysis of molecular marker retention in our radiation hybrid mapping panel allowed the localization
65 ailability of the zebrafish EST database and radiation hybrid mapping panels has dramatically expande
67 iety of human-rodent somatic cell hybrid and radiation hybrid mapping panels, the human SMCC gene was
74 ion, RGD provides tools for gene prediction, radiation hybrid mapping, polymorphic marker selection a
80 the BAC contig with a map of loci ordered by radiation hybrid mapping suggested the most likely genom
81 ed on fluorescence in situ hybridization and radiation hybrid mapping, the human gene has been locali
87 13 by fluorescence in situ hybridization and radiation hybrid mapping; the cDNA for the human homolog
90 to metaphase chromosomes and by whole genome radiation hybrid mapping to chromosome 1p36.1 between DI
94 lop two new types of models for whole-genome radiation hybrid mapping using the general multipoint fr
98 stimulated peripheral blood lymphocytes and radiation hybrid mapping were used for localization of t
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