Found: 10
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Genetic testing for adult-type hypolactasia in Italian families.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2008, v. 46, n. 7, p. 980, doi. 10.1515/CCLM.2008.189
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- Article
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk.
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- Experimental Dermatology, 2020, v. 29, n. 10, p. 980, doi. 10.1111/exd.14163
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- Article
A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals.
- Published in:
- Human Genetics, 2000, v. 106, n. 2, p. 172, doi. 10.1007/s004390051025
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- Article
Haplotype block structure study of the CFTR gene. Most variants are associated with the M470 allele in several European populations.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 85, doi. 10.1038/sj.ejhg.5201498
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- Article
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene.
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- European Journal of Human Genetics, 2005, v. 13, n. 2, p. 184, doi. 10.1038/sj.ejhg.5201306
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- Article
Comment on ‘CFTR gene mutations in sarcoidosis’.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 553, doi. 10.1038/sj.ejhg.5201003
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- Article
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia.
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- European Journal of Human Genetics, 2003, v. 11, n. 1, p. 93, doi. 10.1038/sj.ejhg.5200927
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- Article
Increased frequency of CFTR gene mutations in sarcoidosis: a case/control association study.
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- European Journal of Human Genetics, 2000, v. 8, n. 9, p. 717, doi. 10.1038/sj.ejhg.5200524
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- Article
IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patients.
- Published in:
- Rhinology, 2015, v. 53, n. 4, p. 359, doi. 10.4193/Rhin14.229
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- Article
An Interleukin 13 Polymorphism Is Associated with Symptom Severity in Adult Subjects with Ever Asthma.
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- PLoS ONE, 2016, v. 11, n. 3, p. 1, doi. 10.1371/journal.pone.0151292
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- Article