Found: 7
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Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of lynch syndrome patients.
- Published in:
- Human Mutation, 2010, v. 31, n. 5, p. 578, doi. 10.1002/humu.21229
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- Article
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
- Published in:
- Human Mutation, 2006, v. 27, n. 7, p. 654, doi. 10.1002/humu.20340
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- Article
Am I My Family's Keeper? Disclosure Dilemmas in Next-Generation Sequencing.
- Published in:
- Human Mutation, 2016, v. 37, n. 12, p. 1257, doi. 10.1002/humu.23118
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- Article
Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 3, p. 221, doi. 10.1093/hmg/10.3.221
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- Article
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 9, p. 1769, doi. 10.1093/hmg/8.9.1769
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- Article
Improved overall survival after contralateral risk-reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: A prospective analysis.
- Published in:
- International Journal of Cancer, 2015, v. 136, n. 3, p. 668, doi. 10.1002/ijc.29032
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- Article
CDH1-related hereditary diffuse gastric cancer syndrome: Clinical variations and implications for counseling.
- Published in:
- International Journal of Cancer, 2012, v. 131, n. 2, p. 367, doi. 10.1002/ijc.26398
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- Article