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1 izophrenia of the 22q11.2 deletions found in velo-cardio-facial syndrome.
2 ychiatric illness in patients diagnosed with velo-cardio-facial syndrome, a genetic syndrome that inv
3 port an unusually strong association between velo-cardio-facial syndrome and early-onset bipolar diso
4 unctions of armadillo repeat gene deleted in velo-cardio-facial syndrome (ARVCF) and p120 catenins in
5 ene for 22q11.2 deletion syndrome (DiGeorge/ Velo-cardio-facial syndrome) characterized by facial def
6 r candidate gene for del22q11.2 (DiGeorge or velo-cardio-facial) syndrome, characterized by craniofac
7                   The expansive phenotype of velo-cardio-facial syndrome continues to grow with new b
8                                              Velo-cardio-facial syndrome/DiGeorge syndrome (VCFS/DGS)
9 1.1 repeats are deleted in most persons with velo-cardio-facial syndrome/DiGeorge syndrome (VCFS/DGS)
10                                              Velo-cardio-facial syndrome/DiGeorge syndrome (VCFS/DGS)
11 at-eye syndrome (CES), der(22) syndrome, and velo-cardio-facial syndrome/DiGeorge syndrome (VCFS/DGS)
12 orders, cat-eye syndrome, der() syndrome and velo-cardio-facial syndrome/DiGeorge syndrome (VCFS/DGS)
13 eted in another congenital anomaly disorder, velo-cardio-facial syndrome/DiGeorge syndrome (VCFS/DGS)
14 nscription factor, and an important gene for velo-cardio-facial syndrome/DiGeorge syndrome (VCFS/DGS)
15                                              Velo-cardio-facial syndrome/DiGeorge syndrome results fr
16                 The 22q11 deletion (22q11DS; velo-cardio-facial syndrome/DiGeorge syndrome) is charac
17 te chromosome rearrangements associated with velo-cardio-facial syndrome/DiGeorge syndrome, der(22) s
18                                              Velo-cardio-facial syndrome/DiGeorge syndrome/22q11.2 de
19                                              Velo-cardio-facial syndrome has an expansive phenotype,
20                                              Velo-cardio-facial syndrome has emerged from obscurity t
21 h 22q11 deletion syndrome (22q11DS; DiGeorge/velo-cardio-facial syndrome) have multiple congenital ma
22 that encompass most features of DiGeorge and Velo-Cardio-Facial syndromes in humans.
23 ) of this unselected series of patients with velo-cardio-facial syndrome met DSM-III-R criteria for a
24                               In people with velo-cardio-facial syndrome [or 22q11.2 deletion syndrom
25                                              Velo-cardio-facial syndrome (VCFS) and DiGeorge syndrome
26                                              Velo-cardio-facial syndrome (VCFS) and DiGeorge syndrome
27                                              Velo-cardio-facial syndrome (VCFS) and DiGeorge syndrome
28                                              Velo-cardio-facial syndrome (VCFS) and DiGeorge syndrome
29 of patients with DiGeorge syndrome (DGS) and velo-cardio-facial syndrome (VCFS) have a microdeletion
30                                              Velo-cardio-facial syndrome (VCFS) is a relatively commo
31                                              Velo-cardio-facial syndrome (VCFS) is characterized by c
32                                              Velo-cardio-facial syndrome (VCFS) is the most common mi
33                                              Velo-cardio-facial syndrome (VCFS), a syndrome character
34                                              Velo-cardio-facial syndrome (VCFS), the most frequent kn
35 1), which causes DiGeorge syndrome (DGS) and velo-cardio-facial syndrome (VCFS).
36                                          The velo-cardio-facial syndrome (VCFS)/DiGeorge syndrome (DG
37                                              Velo-cardio-facial syndrome (VCFS)/DiGeorge syndrome (DG
38 etion syndrome (22q11.2DS, DiGeorge syndrome/Velo-cardio-facial syndrome), whose phenotypes include c
39                        Intensive scrutiny of velo-cardio-facial syndrome will undoubtedly continue fo

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