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1 ent length polymorphisms and the others were simple sequence length polymorphisms.
2 ed to a zebrafish genetic linkage map by 102 simple sequence length polymorphisms.
3 es and ESTs and 616 previously characterized simple-sequence length polymorphisms.
4                                              Simple sequence length polymorphism analysis of (C57BL/6
5                                        Using simple sequence length polymorphism analysis, we have ma
6   We used 106 polymorphic markers to perform simple sequence-length polymorphism analysis on F2 hybri
7 ess, we used endogenous proviral markers and simple-sequence length polymorphism analysis to screen A
8 estriction fragment length polymorphisms and simple sequence length polymorphisms in 131 backcross an
9 kers, consisting of 6,580 highly informative simple sequence length polymorphisms integrated with 797
10           We selected a minimal panel of 149 simple sequence length polymorphism markers for a first-
11 cross to construct a detailed genetic map of simple sequence length polymorphism markers within a 6.3
12  Characterization of the LN54 panel with 849 simple sequence length polymorphism markers, 84 cloned g
13 inkage map of the rat genome integrating 767 simple sequence length polymorphism markers, combined ov
14                                        Using simple sequence length polymorphism markers, the rocker
15 ate through 51 clones carrying both gene and simple sequence length polymorphism markers.
16 and F2 mice were analyzed for 70 informative simple sequence length polymorphism markers.
17 rafish genetic linkage map consisting of 705 simple sequence-length polymorphism markers (SSLPs).
18 20 and interval mapping techniques using 159 simple sequence-length polymorphism markers were used to
19 udy, family-based association analysis of 36 simple sequence-length-polymorphism markers and of 17 SN
20 than other types of genetic markers (such as simple-sequence length polymorphisms or microsatellites)
21 394 SNPs as an alternative to analyses using simple sequence length polymorphism (SSLP) marker mappin
22 es, we selected a subset of the extant mouse simple sequence length polymorphism (SSLP) marker set fo
23                           Sixty-five D18Mit- simple sequence length polymorphism (SSLP) markers form
24 p for Xenopus tropicalis, consisting of 2886 Simple Sequence Length Polymorphism (SSLP) markers.
25 DNA from embryos was analyzed at informative simple sequence length polymorphism (SSLP) markers.
26 N and FHH x ACI), containing a total of 4736 simple sequence length polymorphism (SSLP) markers.
27         All 327 rats were genotyped with the simple sequence-length polymorphism (SSLP) markers close
28  this complex using all of the available Mit simple-sequence length polymorphism (SSLP) markers.
29  primers to generate novel, PCR amplifiable, simple sequence length polymorphisms (SSLPs) from yeast
30 t level of genome coverage provided by these simple sequence length polymorphisms (SSLPs) in rice is
31                          Most loci (93%) are simple sequence length polymorphisms (SSLPs) taken from
32 al other labs, we have doubled the number of simple sequence length polymorphisms (SSLPs), genes, exp
33 notypic markers (Pit1dw and Kcnj6wv), and 87 simple sequence length polymorphisms (SSLPs).
34 nthesized and used in PCR assays to test for simple sequence length polymorphisms (SSLPs).
35                                              Simple sequence length polymorphisms (SSLPs, or microsat
36 others, we also scored 593 previously mapped simple-sequence length polymorphisms (SSLPs) in the mapp
37 rkers were also analyzed for LOH by PCR with simple-sequence length polymorphisms (SSLPs); one additi
38    Further, using a novel method to identify simple sequence length polymorphisms, we have developed

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