Found: 6
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Familial occurrence of primary glomerulonephritis: evidence for a role of genetic factors.
- Published in:
- Nephrology Dialysis Transplantation, 1992, v. 7, n. 7, p. 587
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- Publication type:
- Article
HLA Haplotypes and Hormonal Studies in 25 Italian Families of Patients with Classical and Non-classical 21-OH Deficiency.
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- Journal of Pediatric Endocrinology & Metabolism, 1994, v. 7, n. 4, p. 349, doi. 10.1515/jpem.1994.7.4.349
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- Publication type:
- Article
Genetic, immunologic, and environmental heterogeneity of IDDM. Incidence and 12-mo follow-up of an Italian population.
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- 1987
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- Publication type:
- journal article
Distribution of Tumor Necrosis Factor Alleles (Ncol RFLP) and their Relationship to HLA Haplotypes in an Italian Population.
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- Human Heredity, 1993, v. 43, n. 2, p. 103, doi. 10.1159/000154125
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- Publication type:
- Article
A unique MSH2 exon 8 deletion accounts for a major portion of all mismatch repair gene mutations in Lynch syndrome families of Sardinian origin.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 2, p. 154, doi. 10.1038/ejhg.2012.150
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- Publication type:
- Article
A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns.
- Published in:
- Familial Cancer, 2014, v. 13, n. 3, p. 401, doi. 10.1007/s10689-014-9726-3
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- Publication type:
- Article