Works matching IS 13899600 AND DT 2005 AND VI 4 AND IP 4
Results: 14
Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures.
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- Familial Cancer, 2005, v. 4, n. 4, p. 295, doi. 10.1007/s10689-005-0658-9
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- Article
MLH1 and MSH2 Mutations in Colombian Families with Hereditary Nonpolyposis Colorectal Cancer (Lynch syndrome) – Description of Four Novel Mutations.
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- Familial Cancer, 2005, v. 4, n. 4, p. 285, doi. 10.1007/s10689-005-4523-7
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- Article
BAP1 and Breast Cancer Risk.
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- Familial Cancer, 2005, v. 4, n. 4, p. 273, doi. 10.1007/s10689-005-2833-4
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Linkage of a Pedigree Drawing Program and Database to a Program for Determining BRCA Mutation Carrier Probability.
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- Familial Cancer, 2005, v. 4, n. 4, p. 313, doi. 10.1007/s10689-005-8849-y
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Key word Index Volume 4.
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- Familial Cancer, 2005, v. 4, n. 4, p. 337, doi. 10.1007/s10689-005-4695-1
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- Article
Neurofibromatosis 2 (NF2) and Malignant Mesothelioma in a Man with a Constitutional NF2 Missense Mutation.
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- Familial Cancer, 2005, v. 4, n. 4, p. 321, doi. 10.1007/s10689-005-0659-8
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- Article
Mutational analysis of hMsh6 in Israeli HNPCC and HNPCC-like Families.
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- Familial Cancer, 2005, v. 4, n. 4, p. 291, doi. 10.1007/s10689-005-1255-7
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- Article
Survival of Patients with Ovarian Cancer due to a Mismatch Repair Defect.
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- Familial Cancer, 2005, v. 4, n. 4, p. 301, doi. 10.1007/s10689-005-6573-2
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- Article
Patient Satisfaction of BRCA1/2 Genetic Testing by Women at High Risk for Breast Cancer Participating in a Prevention Trial.
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- Familial Cancer, 2005, v. 4, n. 4, p. 279, doi. 10.1007/s10689-005-1474-y
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Contents Volume 4.
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- Familial Cancer, 2005, v. 4, n. 4, p. 339, doi. 10.1007/s10689-005-4696-0
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- Article
Acknowledgements.
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- Familial Cancer, 2005, v. 4, n. 4, p. 335, doi. 10.1007/s10689-005-4694-2
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- Article
Behavioral and Economic Impact of a Familial History of Cancers.
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- Familial Cancer, 2005, v. 4, n. 4, p. 307, doi. 10.1007/s10689-005-3143-6
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- Article
Syndrome of Early Onset Colon Cancers, Hematologic Malignancies & Features of Neurofibromatosis in HNPCC Families with Homozygous Mismatch Repair Gene Mutations.
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- Familial Cancer, 2005, v. 4, n. 4, p. 323, doi. 10.1007/s10689-005-8351-6
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- Article
Lack of Germ-line Mutations at the Specific BRCA1-IRIS Coding Sequence in 114 Spanish High-risk Breast/ovarian Families.
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- Familial Cancer, 2005, v. 4, n. 4, p. 317, doi. 10.1007/s10689-005-1236-x
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- Article