Found: 22
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Distribution of RET proto‐oncogene variants in children with appendicitis.
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- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 2, p. 1, doi. 10.1002/mgg3.1864
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- Article
TCF-3, 4 protein expression correlates with β-catenin expression in MSS and MSI-H colorectal cancer from HNPCC patients but not in sporadic colorectal cancers.
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- International Journal of Colorectal Disease, 2010, v. 25, n. 8, p. 931, doi. 10.1007/s00384-010-0959-9
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Association Between TAS2R38 Gene Polymorphisms and Colorectal Cancer Risk: A Case-Control Study in Two Independent Populations of Caucasian Origin.
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- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0020464
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- Article
Complete homozygous deletion of CTSC in an Iranian family with Papillon- Lefèvre syndrome.
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- International Journal of Dermatology, 2014, v. 53, n. 7, p. 885, doi. 10.1111/j.1365-4632.2012.05769.x
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- Article
No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
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- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 587, doi. 10.1038/ejhg.2008.26
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- Article
Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1.
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- European Journal of Human Genetics, 2008, v. 16, n. 1, p. 62, doi. 10.1038/sj.ejhg.5201923
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- Article
RET-protooncogene variants in patients with sporadic neoplasms of the digestive tract and the central nervous system.
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- International Journal of Colorectal Disease, 2011, v. 26, n. 7, p. 835, doi. 10.1007/s00384-011-1150-7
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- Article
Adenoma and colorectal cancer risks in Lynch syndrome, Lynch‐like syndrome and familial colorectal cancer type X.
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- International Journal of Cancer, 2022, v. 150, n. 1, p. 56, doi. 10.1002/ijc.33790
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- Article
Analysis of RET, ZEB2, EDN3 and GDNF Genomic Rearrangements in Central Congenital Hyperventilation Syndrome Patients by Multiplex Ligation-dependent Probe Amplification.
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- Annals of Human Genetics, 2010, v. 74, n. 4, p. 369, doi. 10.1111/j.1469-1809.2010.00577.x
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Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.
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- Carcinogenesis, 2010, v. 31, n. 9, p. 1612, doi. 10.1093/carcin/bgq146
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- Article
Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families.
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- International Journal of Cancer, 2014, v. 135, n. 1, p. 69, doi. 10.1002/ijc.28650
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- Article
Identification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients.
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- International Journal of Cancer, 2011, v. 129, n. 7, p. 1635, doi. 10.1002/ijc.25821
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- Article
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors.
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- Familial Cancer, 2012, v. 11, n. 1, p. 19, doi. 10.1007/s10689-011-9489-z
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- Article
Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study.
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- BMC Gastroenterology, 2010, v. 10, p. 112, doi. 10.1186/1471-230X-10-112
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- Article
Mutational status of KIT and PDGFRA and expression of PDGFRA are not associated with prognosis after curative resection of primary gastrointestinal stromal tumors (GISTs).
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- Journal of Surgical Oncology, 2011, v. 104, n. 1, p. 59, doi. 10.1002/jso.21905
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- Article
Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).
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- Human Molecular Genetics, 2003, v. 12, n. 24, p. 3207, doi. 10.1093/hmg/ddg354
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- Article
Screening for large rearrangements of the BRCA1 gene in German breast or ovarian cancer families using semi-quantitative multiplex PCR method (Communicated by Arupa Ganguly) Online Citation: Human Mutation, Mutation in Brief #625 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/625.pdf)
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- Human Mutation, 2003, v. 22, n. 1, p. 103, doi. 10.1002/humu.9154
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- Article
Screening for large rearrangements of the BRCA1 gene in German breast or ovarian cancer families using semi‐quantitative multiplex PCR methodCommunicated by Arupa GangulyOnline Citation: Human Mutation, Mutation in Brief #625 (2003) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/625.pdf
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- Human Mutation, 2003, v. 22, n. 1, p. 103, doi. 10.1002/humu.9154
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Identification of six novel MSH2 and MLH1 germline mutations in HNPCC (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #592 (2002) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/592.pdf).
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- Human Mutation, 2003, v. 21, n. 4, p. 445, doi. 10.1002/humu.9121
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- Article
Identification of six novel MSH2 and MLH1 germline mutations in HNPCCCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #592 (2002) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/592.pdf.
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- Human Mutation, 2003, v. 21, n. 4, p. 445, doi. 10.1002/humu.9121
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- Article
TLR4 and IL-18 gene variants in aggressive periodontitis.
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- Journal of Clinical Periodontology, 2008, v. 35, n. 12, p. 1020, doi. 10.1111/j.1600-051X.2008.01334.x
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- Article
Functional Cathepsin C mutations cause different Papillon–Lefèvre syndrome phenotypes.
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- Journal of Clinical Periodontology, 2008, v. 35, n. 4, p. 311, doi. 10.1111/j.1600-051X.2008.01201.x
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- Article