| P2093 | author name string | C Eng | |
| P2860 | cites work | PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer | Q27860985 |
| | Cowden's disease. A possible new symptom complex with multiple system involvement | Q28189705 |
| | Human homolog of patched, a candidate gene for the basal cell nevus syndrome | Q28281033 |
| | Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers | Q28306997 |
| | Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome | Q29615538 |
| | Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus. | Q33256073 |
| | Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy? | Q33674349 |
| | Cowden syndrome | Q33675760 |
| | Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients | Q34166560 |
| | Diagnosis of neurofibromatosis I by using tightly linked, flanking DNA markers | Q35197786 |
| | Cowden disease: gene marker studies and measurements of epidermal growth factor | Q35200999 |
| | Cowden syndrome (multiple hamartoma syndrome). | Q40504443 |
| | Cowden disease. Report of a family and review | Q41593956 |
| | Regulation of retinoic acid receptor expression in dermal fibroblasts | Q42498657 |
| | Association between meningioma and Cowden's disease. | Q46005774 |
| | The Bannayan syndrome: an autosomal dominant disorder consisting of macrocephaly, lipomas, hemangiomas, and risk for intracranial tumors. | Q48949016 |
| | The gene for Darier's disease maps to chromosome 12q23-q24.1. | Q52032483 |
| | Localization of the gene for Cowden disease to chromosome 10q22–23 | Q57694734 |
| | Cowden's disease: a cutaneous marker of breast cancer | Q67339601 |
| | Cowden's disease. A case report with analyses at the molecular level | Q67516789 |
| | Lhermitte-duclos disease and cowden disease: A single phakomatosis | Q67924727 |
| | Multiple hamartoma syndrome (Cowden's disease) associated with renal cell carcinoma and primary neuroendocrine carcinoma of the skin (Merkel cell carcinoma) | Q68109392 |
| | The Cowden syndrome: a clinical and genetic study in 21 patients | Q69486172 |
| | Decreased natural killer cell activity in Cowden's syndrome | Q69593427 |
| | Slowly progressive macrocephaly with hamartomas: a new syndrome? | Q69689402 |
| | Proteus syndrome | Q70480797 |
| | Localisation of a gene for Darier's disease | Q71605774 |
| P433 | issue | 2 | |
| P304 | page(s) | 181-192 | |
| P577 | publication date | 1997-06-01 | |
| P1433 | published in | Journal of Genetic Counseling | Q6295247 |
| P1476 | title | Cowden Syndrome | |
| P478 | volume | 6 | |