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Page 1
SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome.
Genes (Basel). 2022 Jan 28;13(2):252. doi: 10.3390/genes13020252.
Genes (Basel). 2022.
PMID: 35205294
Free PMC article.
HLA-G 14 bp deletion/insertion polymorphism in celiac disease.
Fabris A, Segat L, Catamo E, Morgutti M, Vendramin A, Crovella S.
Fabris A, et al. Among authors: vendramin a.
Am J Gastroenterol. 2011 Jan;106(1):139-44. doi: 10.1038/ajg.2010.340. Epub 2010 Sep 7.
Am J Gastroenterol. 2011.
PMID: 20823837
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The missense variation Q705K in CIAS1/NALP3/NLRP3 gene and an NLRP1 haplotype are associated with celiac disease.
Pontillo A, Vendramin A, Catamo E, Fabris A, Crovella S.
Pontillo A, et al. Among authors: vendramin a.
Am J Gastroenterol. 2011 Mar;106(3):539-44. doi: 10.1038/ajg.2010.474. Epub 2011 Jan 18.
Am J Gastroenterol. 2011.
PMID: 21245836
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Evaluation of two commercial and three home-made fixatives for the substitution of formalin: a formaldehyde-free laboratory is possible.
Zanini C, Gerbaudo E, Ercole E, Vendramin A, Forni M.
Zanini C, et al. Among authors: vendramin a.
Environ Health. 2012 Sep 4;11:59. doi: 10.1186/1476-069X-11-59.
Environ Health. 2012.
PMID: 22947094
Free PMC article.
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