Familial cancer syndromes

[1]  J. Weissenbach,et al.  A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10 , 1993, Nature Genetics.

[2]  D. Easton,et al.  The contribution of inherited predisposition to cancer incidence. , 1990, Cancer surveys.

[3]  G. Lenoir,et al.  Familial breast-ovarian cancer locus on chromosome 17q12-q23 , 1991, The Lancet.

[4]  D. Easton,et al.  The clinical and screening age-at-onset distribution for the MEN-2 syndrome. , 1989, American journal of human genetics.

[5]  R. Bast,et al.  A deletion unit on chromosome 17q in epithelial ovarian tumors distal to the familial breast/ovarian cancer locus. , 1993, Cancer research.

[6]  G. T. Watts,et al.  Paget's disease of the nipple after subcutaneous mastectomy for cancer with primary reconstruction. , 1987, Annals of the Royal College of Surgeons of England.

[7]  R. Norum,et al.  Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2. , 1993, Human molecular genetics.

[8]  P. Tonin,et al.  Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12-21: exclusion of candidate genes EDH17B2 and RARA. , 1993, Human molecular genetics.

[9]  A. Weisman,et al.  The Emotional Impact of Recurrent Cancer , 1986 .

[10]  J. Woods,et al.  Surgical alternatives in subcutaneous mastectomy reconstruction. , 1988, Clinics in Plastic Surgery.

[11]  S. Miller,et al.  Analysis of the risk reduction of prophylactic partial mastectomy in Sprague-Dawley rats with 7,12-dimethylbenzanthracene-induced breast cancer. , 1986, Surgery.

[12]  D. Easton,et al.  Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium. , 1993, American journal of human genetics.

[13]  D. Easton,et al.  Allele losses in the region 17q12–21 in familial breast and ovarian cancer involve the wild–type chromosome , 1992, Nature Genetics.

[14]  H. Wolfe,et al.  Familial medullary thyroid carcinoma and C cell hyperplasia. , 1981, Clinics in endocrinology and metabolism.

[15]  R. Eeles Predictive testing for germline mutations in the p53 gene: are all the questions answered? , 1993, European journal of cancer.

[16]  N Risch,et al.  Genetic analysis of breast cancer in the cancer and steroid hormone study. , 1991, American journal of human genetics.

[17]  W. Kimberling,et al.  Genetic predisposition to breast cancer , 1984, Cancer.

[18]  P. Engstrom,et al.  Mammography adherence and psychological distress among women at risk for breast cancer. , 1993, Journal of the National Cancer Institute.

[19]  J. Holland,et al.  Psychological distress and surveillance behaviors of women with a family history of breast cancer. , 1992, Journal of the National Cancer Institute.

[20]  R. Eeles,et al.  Detection of point mutations in the p53 gene: Comparison of single‐strand conformation polymorphism, constant denaturant gel electrophoresis, and hydroxylamine and osmium tetroxide techniques , 1993, Human mutation.

[21]  M. King,et al.  Linkage of early-onset familial breast cancer to chromosome 17q21. , 1990, Science.

[22]  S. Bülow,et al.  Familial polyposis coli. , 1987, Seminars in surgical oncology.

[23]  J. Robbins,et al.  Thyroid cancer: a lethal endocrine neoplasm. , 1991, Annals of internal medicine.

[24]  P. Devilee,et al.  Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions. , 1993, Oncogene.

[25]  A. Ringberg,et al.  A prospective study of psychiatric and psychosocial sequelae of bilateral subcutaneous mastectomy. , 1986, Scandinavian journal of plastic and reconstructive surgery.

[26]  R. Love,et al.  The Cancer Prevention Clinic , 1986 .

[27]  W D Flanders,et al.  The lifetime risk of developing breast cancer. , 1993, Journal of the National Cancer Institute.

[28]  D. Kelsell,et al.  Genetic analysis of the BRCA1 region in a large breast/ovarian family: refinement of the minimal region containing BRCA1. , 1993, Human molecular genetics.

[29]  B. Ponder,et al.  Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A , 1993, Nature.