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1 condition or in syndromic conditions such as Williams-Beuren syndrome.
2 a patient with deletion of elastin owing to Williams-Beuren syndrome.
3 ntribute to certain deficits associated with Williams-Beuren syndrome.
4 niofacial and cognitive abnormalities in the Williams-Beuren syndrome.
5 may help identify molecular determinants of Williams-Beuren syndrome.
6 7q11, the reciprocal of the deletion causing Williams-Beuren syndrome.
7 7q11.23, usually associated with the typical Williams-Beuren syndrome.
8 invariably deleted in the haploinsufficiency Williams-Beuren Syndrome.
9 pment and suggest how it could contribute to Williams-Beuren syndrome.
11 1.23 near the telomeric duplicated region of Williams-Beuren syndrome, a developmental disorder affec
12 ome 7q11.23 that is hemizgygously deleted in Williams-Beuren syndrome, a multisystemic developmental
14 hared and symmetrically opposite phenotypes--Williams-Beuren syndrome and 7q-microduplication syndrom
15 cardiovascular complications associated with Williams-Beuren syndrome and isolated supravalvular aort
16 ation of a girl with a clinical phenotype of Williams-Beuren syndrome, associated with unilateral ant
17 q11.23, where the reciprocal deletion causes Williams-Beuren syndrome, characterized by a highly soci
18 , we isolated a Xenopus homolog of the human Williams-Beuren syndrome critical region 11 (XWBSCR11),
19 we determined the expression profile of the Williams-Beuren syndrome critical region-deleted genes a
21 e, Miller-Dieker lissencephaly syndrome, and Williams-Beuren syndrome--in which the deleted region en
25 ygous microdeletion distally adjacent to the Williams-Beuren syndrome region on chromosome 7q11.23.
27 nd voice hoarsening in a baby diagnosed with Williams-Beuren syndrome that was born premature and req
28 at haploinsufficiency in BEN is causative to Williams-Beuren syndrome, these results may further lead
29 on structure of the PHD motif from the human Williams-Beuren syndrome transcription factor (WSTF) pro
30 one variant H2A.X is phosphorylated by WSTF (Williams-Beuren syndrome transcription factor), a compon
31 a new regulatory mechanism mediated by WSTF (Williams-Beuren syndrome transcription factor, also know
34 copy of a duplicated gene flanking the 2-Mb Williams-Beuren syndrome (WBS) common deletion at 7q11.2
35 rizzled gene, FZD3, now renamed FZD9, in the Williams-Beuren syndrome (WBS) deletion region at chromo
39 t the 7q11.23 region hemizygously deleted in Williams-Beuren syndrome (WBS), a complex multisystemic
45 iniscent of the human microdeletion disorder Williams-Beuren syndrome (WBS); craniofacial imaging rev
47 commonly deleted in patients affected by the Williams-Beuren syndrome, which is a complex neurodevelo
48 or both proteins are deleted in persons with Williams-Beuren syndrome, who often manifest muscle weak
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