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1 e eas(UCLA) allele is associated with a long paracentric inversion.
2 e block that was subsequently disrupted by a paracentric inversion.
3 en 30 breaks as part of 5 translocations, 10 paracentric inversions, 2 pericentric inversions, and 4
4 radiation-induced tumors are associated with paracentric inversions activating the receptor tyrosine
5 origin of the Y-specific 250-kb region in a paracentric inversion after the initial transfer of X DN
6 arrangements, which could be explained by 23 paracentric inversions and five translocations during ev
10 bling species has many polymorphic and fixed paracentric inversions detectable in polytene chromosome
11 tility of the method both by genotyping a Yp paracentric inversion, found in approximately 60% of Nor
14 ich three sibs inherited from their mother a paracentric inversion in the chromosome 7 candidate regi
15 ntenic melon chromosome I suggested that the paracentric inversion in this chromosome occurred during
17 ng the long arms of chromosomes 4 and 5, and paracentric inversions in the long arm of chromosomes 1
18 type in bib is shown to be associated with a paracentric inversion [In(4)ab] on the neo-X chromosome,
19 e to encounter deletions, translocations, or paracentric inversions involving 5q11 to 5q13, which ind
23 We report here a rearrangement of BRAF via paracentric inversion of chromosome 7q resulting in an i
24 y of the gene arrangements are the result of paracentric inversions on both arms of the metacentric s
26 seudoobscura harbors a rich polymorphism for paracentric inversions on the third chromosome, and the
27 element across genus Drosophila species and paracentric inversions serve as the dominant mechanism f
28 We illustrate this method by genotyping a Yp paracentric inversion sponsored by >300-kb-long inverted
29 gested that the a18H mutation results from a paracentric inversion that affects two loci: agouti and
31 2002, a noncoding region tightly linked to a paracentric inversion that strongly contributes to repro
32 e and subsequent rearrangements, including a paracentric inversion, that have taken place within the
33 offset elements may have given rise to many paracentric inversions, thereby contributing to the shuf
34 e MAPK pathway primarily through chromosomal paracentric inversions, whereas in sporadic forms of the
35 tions for prenatal counseling of carriers of paracentric inversions, who typically are considered to
36 We report the first such case involving a paracentric inversion with a breakpoint located approxim
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