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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 invariably deleted in the haploinsufficiency Williams-Beuren Syndrome.
8 pment and suggest how it could contribute to Williams-Beuren syndrome.
9 7q11.23, usually associated with the typical Williams-Beuren syndrome.
10 .21 (48), 16p11.2 (autism, 34), and 7q11.23 (Williams-Beuren syndrome, 11).
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
13                                              Williams-Beuren syndrome (also known as Williams syndrom
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
20 of the primate-specific inversion within the Williams-Beuren syndrome critical region.
21 ng of an individual with severe epilepsy and Williams-Beuren syndrome identified a frameshifting de n
22 e, Miller-Dieker lissencephaly syndrome, and Williams-Beuren syndrome--in which the deleted region en
23                                              Williams-Beuren syndrome is a developmental multisystemi
24                                              Williams-Beuren syndrome is a rare congenital genetic di
25                                              Williams-Beuren syndrome is characterized by mild mental
26 SCR11), one of the genes commonly deleted in Williams-Beuren syndrome patients.
27 ygous microdeletion distally adjacent to the Williams-Beuren syndrome region on chromosome 7q11.23.
28 region on 1q21.1 and duplication at the WBS (Williams-Beuren syndrome) region at 7q11.23.
29 nd voice hoarsening in a baby diagnosed with Williams-Beuren syndrome that was born premature and req
30 at haploinsufficiency in BEN is causative to Williams-Beuren syndrome, these results may further lead
31 on structure of the PHD motif from the human Williams-Beuren syndrome transcription factor (WSTF) pro
32 one variant H2A.X is phosphorylated by WSTF (Williams-Beuren syndrome transcription factor), a compon
33 a new regulatory mechanism mediated by WSTF (Williams-Beuren syndrome transcription factor, also know
34                               A diagnosis of Williams-Beuren syndrome was made based on the microdele
35 opy number variation (CNV) at 7q11.23 causes Williams-Beuren syndrome (WBS) and 7q microduplication s
36              A new study uses the example of Williams-Beuren syndrome (WBS) and Williams-Beuren regio
37  copy of a duplicated gene flanking the 2-Mb Williams-Beuren syndrome (WBS) common deletion at 7q11.2
38 rizzled gene, FZD3, now renamed FZD9, in the Williams-Beuren syndrome (WBS) deletion region at chromo
39                                              Williams-Beuren syndrome (WBS) is a developmental disord
40                                              Williams-Beuren syndrome (WBS) is a microdeletion disord
41                                              Williams-Beuren syndrome (WBS) is a neurodevelopmental d
42                                              Williams-Beuren syndrome (WBS) is a rare disorder caused
43                                              Williams-Beuren syndrome (WBS) is a rare genetic multisy
44                                              Williams-Beuren syndrome (WBS) is a rare genetic neurode
45 t the 7q11.23 region hemizygously deleted in Williams-Beuren syndrome (WBS), a complex multisystemic
46     SVAS severity varies among patients with Williams-Beuren syndrome (WBS), a rare disorder that rem
47                                              Williams-Beuren syndrome (WBS), an autosomal dominant ge
48                                              Williams-Beuren syndrome (WBS), caused by a microdeletio
49              The neurodevelopmental disorder Williams-Beuren syndrome (WBS), is caused by a microdele
50 us deletion of the elastin gene (ELN) causes Williams-Beuren syndrome (WBS), while single nucleotide
51 b region on chromosome 7 which is deleted in Williams-Beuren syndrome (WBS).
52 rtic stenosis (SVAS), and five patients with Williams-Beuren syndrome (WBS).
53 iniscent of the human microdeletion disorder Williams-Beuren syndrome (WBS); craniofacial imaging rev
54                                              Williams-Beuren syndrome (WBS; OMIM 194050) is caused by
55 commonly deleted in patients affected by the Williams-Beuren syndrome, which is a complex neurodevelo
56 or both proteins are deleted in persons with Williams-Beuren syndrome, who often manifest muscle weak