218 results on '"Menko, F H"'
Search Results
52. A case of loss of heterozygosity in the BRCA2 gene of a borderline ovarian tumor: case report and review of literature
53. Re: Germline BRCA1 Mutations and a Basal Epithelial Phenotype in Breast Cancer
54. PROPHYLACTIC SURGERY IN WOMEN AT HIGH RISK FOR BREAST AND/OR OVARIAN/TUBAL CANCER
55. HUMORAL IMMUNE RESPONSES TO MUC1 IN WOMEN WITH BRCA1/BRCA2 MUTATIONS
56. Histopathologic Features of Genetically Determined Ovarian Cancer
57. Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach
58. Atypical MEN Type 2B Associated with Two Germline RET Mutations on the Same Allele Not Involving Codon 918
59. Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2
60. The risk of brain tumours in hereditary non-polyposis colorectal cancer (HNPCC)
61. Clinical heterogeneity of familial colorectal cancer and its influence on screening protocols.
62. Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype.
63. Reply to Dr. Qumsiyeh
64. A giant congenital orbital tumor: An unusual presentation of retinoblastoma
65. Robin sequence and a deficiency of the left forearm in a girl with a deletion of chromosome 4q33-qter
66. Williams syndrome and chromosome 18.
67. Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcifications.
68. Genetic counseling for hereditary cancer: A pilot study on experiences of patients and family members
69. Erratum: Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis (Gastroenterology (1996) 110 (1020- 1027))
70. Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method
71. Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis
72. HIF-1 alpha overexpression in ductal carcinoma in situ of the breast in hereditary predisposed women
73. Differences between hereditary and sporadic ovarian cancer
74. Familial Benign Hypercalcaemia: STUDY OF A LARGE FAMILY
75. Humoral immune responses to MUC1 in women with a BRCA1 or BRCA2 mutation.
76. [DNA-based diagnosis of hereditary tumour predisposition].
77. [Recommendations for the management of women with an increased genetic risk of gynaecological cancer].
78. Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer.
79. Comparative genomic hybridization of microdissected familial ovarian carcinoma: two deleted regions on chromosome 15q not previously identified in sporadic ovarian carcinoma.
80. [Patient with Peutz-Jeghers syndrome and liver metastases from an unknown primary tumor].
81. Molecular evidence linking primary cancer of the fallopian tube to BRCA1 germline mutations.
82. Familial breast cancer: clinical services in The Netherlands.
83. [Two patients with Muir-Torre syndrome].
84. [Periodic colonoscopic examinations of persons with a positive family history for colorectal cancer. Work Group 'Hereditary non-polyposis- colon-rectum cancers'].
85. [Genetics of colorectal cancer. II. Hereditary background of sporadic and familial colorectal cancer].
86. [Genetics of colorectal cancer. I. Non-polyposis and polyposis forms of hereditary colorectal cancer].
87. A cost-effectiveness analysis of colorectal screening of hereditary nonpolyposis colorectal carcinoma gene carriers.
88. [Hereditary mutations in the p53 tumor suppressor gene; significance for clinical practice. National Work Group Hereditary Mamma Carcinoma].
89. Inheritance of abnormal expression of SOS-like response in xeroderma pigmentosum and hereditary cancer-prone syndromes.
90. A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch family.
91. Genetic counseling in hereditary nonpolyposis colorectal cancer.
92. Hereditary nonpolyposis colorectal cancer: results of long-term surveillance in 50 families.
93. The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region.
94. Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis.
95. Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer.
96. [The chance of breast carcinoma and related carcinomas in a positive family anamnesis. Landelijke Werkgroep Erfelijk Mammacarcinoom van de Stichting Opsporing Erfelijke Tumoren].
97. [Cloning of the first gene for breast/ovarian cancer (BRCA1), mapping of a second gene locus (BRCA2) and consequences for clinical practice].
98. Endometrial cancer in four sisters: report of a kindred with presumed cancer family syndrome.
99. [Familial ovarian carcinoma].
100. Variable age of onset in hereditary nonpolyposis colorectal cancer: clinical implications.
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