Found: 22
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A Genetic Basis for the Inviability of Hybrids Between Sibling Species of Drosophila.
- Published in:
- Genetics, 1990, v. 124, n. 4, p. 909
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- Publication type:
- Article
Excess of hMLH1 germline mutations in Swiss families with hereditary non-polyposis colorectal cancer.
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- International Journal of Cancer, 1998, v. 78, n. 6, p. 680, doi. 10.1002/(SICI)1097-0215(19981209)78:6<680::AID-IJC3>3.0.CO;2-U
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- Article
Double frameshift mutations in APC and MSH2 in the same individual.
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- 2007
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- Publication type:
- Correction Notice
Double frameshift mutations in APC and MSH2 in the same individual.
- Published in:
- International Journal of Colorectal Disease, 2006, v. 21, n. 1, p. 79, doi. 10.1007/s00384-005-0772-z
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- Publication type:
- Article
Double frameshift mutations in APC and MSH2 in the same individual.
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- International Journal of Colorectal Disease, 2005, v. 20, n. 5, p. 466, doi. 10.1007/s00384-005-0764-z
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- Publication type:
- Article
Evidence for genetic anticipation in hereditary non-polyposis colorectal cancer.
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- Human Genetics, 2005, v. 116, n. 6, p. 461, doi. 10.1007/s00439-005-1272-5
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- Publication type:
- Article
Differential rates of frameshift alterations in four repeat sequences of hereditary nonpolyposis colorectal cancer tumors.
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- Human Genetics, 2002, v. 111, n. 3, p. 284, doi. 10.1007/s00439-002-0789-0
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- Publication type:
- Article
The murine orthologue of the Golgi-localized TPTE protein provides clues to the evolutionary history of the human TPTE gene family.
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- Human Genetics, 2001, v. 109, n. 6, p. 569, doi. 10.1007/s004390100607
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- Publication type:
- Article
Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012.
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- European Journal of Human Genetics, 2013, v. 21, n. 1, p. 00, doi. 10.1038/ejhg.2012.164
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- Publication type:
- Article
Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2).
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- European Journal of Human Genetics, 2010, v. 18, n. 9, p. -1, doi. 10.1038/ejhg.2009.232
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- Article
‘Exceptional sons’ from Drosophila melanogaster mothers carrying a balancer X chromosome.
- Published in:
- Genetics Research, 1990, v. 55, n. 3, p. 159, doi. 10.1017/S0016672300025477
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- Publication type:
- Article
Prevalence of MYH germline mutations in Swiss APC mutation-negative polyposis patients.
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- International Journal of Cancer, 2006, v. 118, n. 8, p. 1937, doi. 10.1002/ijc.21470
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- Publication type:
- Article
A new bioinformatics tool to help assess the significance of <italic>BRCA1</italic> variants.
- Published in:
- Human Genomics, 2018, v. 12, n. 1, p. N.PAG, doi. 10.1186/s40246-018-0168-0
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- Publication type:
- Article
X-linked small GTPase and OXPHOS genes are candidates for the genetic basis of hybrid inviability in Drosophila.
- Published in:
- Development Genes & Evolution, 2002, v. 212, n. 10, p. 504, doi. 10.1007/s00427-002-0271-y
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- Publication type:
- Article
Selection of patients with germline MLH1 mutated Lynch syndrome by determination of MLH1 methylation and BRAF mutation.
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- Familial Cancer, 2010, v. 9, n. 2, p. 167, doi. 10.1007/s10689-009-9302-4
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- Publication type:
- Article
Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC).
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 123, doi. 10.1002/gcc.20219
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- Publication type:
- Article
Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers.
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- Journal of Cancer Epidemiology, 2009, p. 1, doi. 10.1155/2009/791754
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- Publication type:
- Article
High-Resolution Breakpoint Analysis Provides Evidence for the Sequence-Directed Nature of Genome Rearrangements in Hereditary Disorders.
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- Human Mutation, 2015, v. 36, n. 2, p. 250, doi. 10.1002/humu.22734
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- Publication type:
- Article
The educational role of external quality assessment in genetic testing: a 7-year experience of the European Molecular Genetics Quality Network (EMQN) in Lynch syndrome.
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- Human Mutation, 2011, v. 32, n. 6, p. 696, doi. 10.1002/humu.21493
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- Publication type:
- Article
Distinct patterns of germ-line deletions in MLH1 and MSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC).
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- Human Mutation, 2006, v. 27, n. 4, p. 388, doi. 10.1002/humu.9417
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- Article
Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells.
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- Human Molecular Genetics, 1994, v. 3, n. 7, p. 1035
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- Publication type:
- Article
Exon skipping associated with A→G transition at +4 of the IVS33 splice donor site of the neurofibromatosis type 1 (NF1) gene.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 4, p. 663
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- Publication type:
- Article