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PubCasesCollection
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# proj.
# Ann.
updated_at
PubMed
21684788
Large contiguous gene deletions in Sjögren-Larsson syndrome. Sjögren-Larsson syndrome (SLS) is an au
1.5 KB
2015-11-26
32
0
-
PubMed
1429602
An amino acid substitution (Gly853-->Glu) in the collagen alpha 1(II) chain produces hypochondrogene
1.6 KB
2015-11-18
31
0
-
PubMed
2788166
Molecular basis of the liver and lung disease associated with the alpha 1-antitrypsin deficiency all
2.39 KB
2015-11-26
31
0
-
PubMed
19208385
Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with muta
890 Bytes
2017-09-04
31
0
-
PubMed
16720068
Possible neuroleptic malignant syndrome related to concomitant treatment with paroxetine and alprazo
1.72 KB
2017-09-11
31
0
-
PubMed
24014394
A homozygous mutation in LYRM7/MZM1L associated with early onset encephalopathy, lactic acidosis, an
1.16 KB
2015-11-26
31
0
-
PubMed
22836123
Late-onset scleroderma renal crisis induced by tacrolimus and prednisolone: a case report. Scleroder
646 Bytes
2016-01-05
31
0
-
PubMed
17297207
Quinine-induced arrhythmia in a patient with severe malaria. It was reported that there was a case o
1.92 KB
2015-12-28
31
0
-
PubMed
21126715
A Taiwanese boy with congenital generalized lipodystrophy caused by homozygous Ile262fs mutation in
1.4 KB
2015-11-25
31
0
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PubMed
18681856
Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation
1.58 KB
2015-08-06
31
0
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