| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1005940820 |
| P356 | DOI | 10.1007/S10689-014-9752-1 |
| P8608 | Fatcat ID | release_pyqq4sltcrg2jidbvlukbhurmi |
| P698 | PubMed publication ID | 25287320 |
| P50 | author | Ingrid Winship | Q40391308 |
| Brigitte Bressac-de Paillerets | Q43376253 | ||
| P2093 | author name string | Marine Guillaud-Bataille | |
| Kirsty Mann | |||
| Jill Magee | |||
| Christophe Blondel | |||
| Josie Yeatman | |||
| P2860 | cites work | The 2007 WHO classification of tumours of the central nervous system | Q24685772 |
| Mutations in SUFU predispose to medulloblastoma | Q34133729 | ||
| Loss of Trp53 promotes medulloblastoma development but not skin tumorigenesis in Sufu heterozygous mutant mice | Q35605827 | ||
| The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma | Q35993240 | ||
| Loss of SUFU function in familial multiple meningioma. | Q36439334 | ||
| Lessons from the skin--cutaneous features of familial cancer | Q37153048 | ||
| High frequency of germline SUFU mutations in children with desmoplastic/nodular medulloblastoma younger than 3 years of age. | Q42504937 | ||
| Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation | Q42510080 | ||
| Kif7 regulates Gli2 through Sufu-dependent and -independent functions during skin development and tumorigenesis | Q42513668 | ||
| Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma | Q46959964 | ||
| Identification of a SUFU germline mutation in a family with Gorlin syndrome. | Q51932422 | ||
| Loss of suppressor-of-fused function promotes tumorigenesis. | Q53334228 | ||
| Birt-Hogg-Dubé syndrome: a novel marker of kidney neoplasia. | Q55033345 | ||
| Retrospective family study of childhood medulloblastoma. | Q55471502 | ||
| Incomplete penetrance of the predisposition to medulloblastoma associated with germ-line SUFU mutations | Q60035710 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 151-155 | |
| P577 | publication date | 2015-03-01 | |
| P1433 | published in | Familial Cancer | Q15761917 |
| P1476 | title | Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndrome. | |
| P478 | volume | 14 |
| Q38887259 | Cohort study of Gorlin syndrome with emphasis on standardised phenotyping and quality of life assessment. |
| Q49548506 | Germline SUFU mutation carriers and medulloblastoma: clinical characteristics, cancer risk and prognosis. |
| Q55249441 | Molecular mechanisms of suppressor of fused in regulating the hedgehog signalling pathway. |
| Q48194288 | Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same. |
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