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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1981 | 1 |
2000 | 1 |
2002 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 387974
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A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis.
Am J Hum Genet. 2002 Dec;71(6):1443-9. doi: 10.1086/344580. Epub 2002 Nov 4.
Am J Hum Genet. 2002.
PMID: 12417987
Free PMC article.
Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.
Bétard C, Rasquin-Weber A, Brewer C, Drouin E, Clark S, Verner A, Darmond-Zwaig C, Fortin J, Mercier J, Chagnon P, Fujiwara TM, Morgan K, Richter A, Hudson TJ, Mitchell GA.
Bétard C, et al.
Am J Hum Genet. 2000 Jul;67(1):222-8. doi: 10.1086/302993. Epub 2000 May 11.
Am J Hum Genet. 2000.
PMID: 10820129
Free PMC article.
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Severe familial cholestasis in North American Indian children: a clinical model of microfilament dysfunction?
Weber AM, Tuchweber B, Yousef I, Brochu P, Turgeon C, Gabbiani G, Morin CL, Roy CC.
Weber AM, et al.
Gastroenterology. 1981 Oct;81(4):653-62.
Gastroenterology. 1981.
PMID: 6894906
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