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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
9 1.1 repeats are deleted in most persons with 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)
17 te chromosome rearrangements associated with velo-cardio-facial syndrome/DiGeorge syndrome, der(22) s
21 h 22q11 deletion syndrome (22q11DS; DiGeorge/velo-cardio-facial syndrome) have multiple congenital ma
23 ) of this unselected series of patients with velo-cardio-facial syndrome met DSM-III-R criteria for a
29 of patients with DiGeorge syndrome (DGS) and velo-cardio-facial syndrome (VCFS) have a microdeletion
38 etion syndrome (22q11.2DS, DiGeorge syndrome/Velo-cardio-facial syndrome), whose phenotypes include c
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