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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1979 | 1 |
1990 | 2 |
1994 | 1 |
1995 | 1 |
2004 | 1 |
2023 | 0 |
PubMed (OMIM) for id: 1647210
6 results
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Page 1
Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome.
Nat Genet. 2004 Apr;36(4):400-4. doi: 10.1038/ng1325. Epub 2004 Mar 28.
Nat Genet. 2004.
PMID: 15052268
Arthrogryposis, renal dysfunction and cholestasis syndrome: report of five patients from three Italian families.
Di Rocco M, Callea F, Pollice B, Faraci M, Campiani F, Borrone C.
Di Rocco M, et al.
Eur J Pediatr. 1995 Oct;154(10):835-9. doi: 10.1007/BF01959793.
Eur J Pediatr. 1995.
PMID: 8529684
Review.
Item in Clipboard
Liver histology in the arthrogryposis multiplex congenita, renal dysfunction, and cholestasis (ARC) syndrome: report of three new cases and review.
Horslen SP, Quarrell OW, Tanner MS.
Horslen SP, et al.
J Med Genet. 1994 Jan;31(1):62-4. doi: 10.1136/jmg.31.1.62.
J Med Genet. 1994.
PMID: 8151641
Free PMC article.
Review.
Item in Clipboard
Arthrogryposis, cholestatic pigmentary liver disease and renal dysfunction: report of a second family.
Di Rocco M, Reboa E, Barabino A, Larnaout A, Canepa M, Savioli C, Cremonte M, Borrone C.
Di Rocco M, et al.
Am J Med Genet. 1990 Oct;37(2):237-40. doi: 10.1002/ajmg.1320370214.
Am J Med Genet. 1990.
PMID: 2248291
Item in Clipboard
Arthrogryposis multiplex congenita with renal and hepatic abnormalities in a female infant.
Saraiva JM, Lemos C, Gonçalves I, Carneiro F, Mota HC.
Saraiva JM, et al.
J Pediatr. 1990 Nov;117(5):761-3. doi: 10.1016/s0022-3476(05)83339-6.
J Pediatr. 1990.
PMID: 2231211
No abstract available.
Item in Clipboard
A lethal familial syndrome associating arthrogryposis multiplex congenita, renal dysfunction, and a cholestatic and pigmentary liver disease.
Nezelof C, Dupart MC, Jaubert F, Eliachar E.
Nezelof C, et al.
J Pediatr. 1979 Feb;94(2):258-60. doi: 10.1016/s0022-3476(79)80839-2.
J Pediatr. 1979.
PMID: 762621
No abstract available.
Item in Clipboard
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