| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/0140-6736(92)90868-4 |
| P698 | PubMed publication ID | 1347096 |
| P50 | author | Gareth Evans | Q29642643 |
| P2093 | author name string | M W Kilpatrick | |
| P A Farndon | |||
| R G Del Mastro | |||
| P433 | issue | 8793 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 2 | |
| P304 | page(s) | 581-582 | |
| P577 | publication date | 1992-03-01 | |
| P1433 | published in | The Lancet | Q939416 |
| P1476 | title | Location of gene for Gorlin syndrome | |
| P478 | volume | 339 |
| Q36676778 | A Rare Case of a Symptomatic Tumor Found in the Groin Area: An Atypical Location Unexposed to the Known Causes |
| Q42495602 | A patient with naevoid basal cell carcinoma syndrome and Turner's syndrome. |
| Q36732493 | A review of hedgehog signaling in cranial bone development |
| Q42497462 | A sebaceous nevus in a child with the nevoid basal cell carcinoma syndrome |
| Q33680852 | A survey of phenotypic features in juvenile polyposis |
| Q35555946 | Acute abdominal pain with a calcified pelvic mass |
| Q42462616 | An ultrasound analysis of the response of Gorlin syndrome-related and sporadic basal cell carcinomas to aminolaevulinic acid photodynamic therapy |
| Q40537466 | Analysis of four microsatellite markers on the long arm of chromosome 9 by meiotic recombination in flow-sorted single sperm. |
| Q42480064 | Anomalous Extraocular Muscles with Strabismus |
| Q35194185 | Association of the widespread A149P hereditary fructose intolerance mutation with newly identified sequence polymorphisms in the aldolase B gene |
| Q42505133 | Basal cell carcinoma of the eyelid associated with Gorlin-Goltz syndrome |
| Q34442671 | Basal cell carcinoma of the head and neck |
| Q35652710 | Basal cell carcinoma: pathogenesis, epidemiology, clinical features, diagnosis, histopathology, and management |
| Q42455374 | Basal cell carcinomas developing in a case of medulloblastoma associated with Gorlin's syndrome. |
| Q42523671 | Bilateral hyperplasia of the mandibular coronoid processes in patients with nevoid basal cell carcinoma syndrome: an undescribed sign |
| Q31146746 | Calcification of the falx cerebri. A pathognomonic symptom of Gorlin-Goltz syndrome |
| Q36406904 | Cancer Surveillance in Gorlin Syndrome and Rhabdoid Tumor Predisposition Syndrome |
| Q42441900 | Cellular proliferation characteristics of basal cell carcinoma: relationship to clinical subtype and histopathology. |
| Q34259606 | Chromosomal assignment of a gene encoding a new collagen type (COL15A1) to 9q21 --> q22. |
| Q34783428 | Classifying the medulloblastoma: insights from morphology and molecular genetics |
| Q42511026 | Clinical manifestations and treatment for keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome: a study in 25 Japanese patients |
| Q38413862 | Clinical utility gene card for: Gorlin syndrome |
| Q42519992 | Clinical utility gene card for: Gorlin syndrome--update 2013 |
| Q38887259 | Cohort study of Gorlin syndrome with emphasis on standardised phenotyping and quality of life assessment. |
| Q42526105 | Complex karyotypic abnormality in ovarian fibroma associated with Gorlin syndrome |
| Q33595421 | Complications of the naevoid basal cell carcinoma syndrome: results of a population based study |
| Q35796194 | Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas |
| Q34634737 | Cystic lesions of the jaws - a clinicopathological study of 322 cases and review of the literature |
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| Q88371763 | Familial Syndromes Involving Meningiomas Provide Mechanistic Insight Into Sporadic Disease |
| Q34480137 | Familial neurogenic tumor syndromes |
| Q47416952 | Familial sarcoma: challenging pedigrees |
| Q42510188 | Fine needle aspiration cytology as an additional tool in the diagnosis of odontogenic keratocyst. |
| Q35195046 | Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity. |
| Q36142459 | Genetic and molecular alterations across medulloblastoma subgroups |
| Q33596205 | Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families |
| Q37737307 | Genetics of medulloblastoma: clues for novel therapies |
| Q40686977 | Genetics of primary brain tumors: a review |
| Q35447362 | Genetics of skin appendage neoplasms and related syndromes |
| Q41196588 | Genetics of the nevoid basal cell carcinoma syndrome. |
| Q36247721 | Genome-Wide Association Studies of Multiple Keratinocyte Cancers |
| Q77538121 | Genomic gains and losses are similar in genetic and histologic subsets of rhabdomyosarcoma, whereas amplification predominates in embryonal with anaplasia and alveolar subtypes |
| Q42465346 | Gorlin syndrome with bilateral polydactyly: a rare case report |
| Q36265088 | Gorlin's syndrome - Report of a case and management of cystic lesions |
| Q36956923 | Gorlin's syndrome presenting with myolipoma of tongue base |
| Q42445405 | Gorlin's syndrome: diffuse appendicular skeletal involvement with scintigraphic correlation |
| Q84298183 | Gorlin-Goltz Syndrome with Intracranial Meningioma: Case Report and Review of Literature |
| Q36180212 | Gorlin-Goltz Syndrome: Case report and literature review |
| Q35184068 | Gorlin-Goltz syndrome |
| Q36246237 | Gorlin-Goltz syndrome: A case series of 5 patients in North Indian population with comparative analysis of literature |
| Q42464678 | Gorlin-Goltz syndrome: a 25-year follow-up of a familial case |
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| Q42489235 | Heterozygous PTCH1 Mutations Impact the Bone Metabolism in Patients With Nevoid Basal Cell Carcinoma Syndrome Likely by Regulating SPARC Expression |
| Q42496132 | Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree |
| Q34763576 | Imbalances of chromosomes 4, 9, and 12 are recurrent in the thecoma-fibroma group of ovarian stromal tumors |
| Q40912548 | Increase in nucleoli after x-radiation of fibroblasts of patients with Gorlin syndrome |
| Q37299488 | Inherited disorders as a risk factor and predictor of neurodevelopmental outcome in pediatric cancer |
| Q41236837 | Interphase cytogenetic analysis of solid tumors by non-isotopic DNA in situ hybridization |
| Q42489597 | Is PATCHED an important candidate gene for neural tube defects? Cranial and thoracic neural tube defects in a family with Gorlin syndrome: a case report |
| Q49222435 | Isochromosome (17)(q10) as the sole structural chromosomal rearrangement in a case of botryoid rhabdomyosarcoma |
| Q37153048 | Lessons from the skin--cutaneous features of familial cancer |
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| Q90734441 | Long-term Response to Vismodegib in a Patient with Gorlin-Goltz Syndrome: A Case Report and Review of Pathological Mechanisms Involved |
| Q39991093 | Loss of heterozygosity analysis of keratoacanthoma reveals multiple differences from cutaneous squamous cell carcinoma |
| Q36590533 | Loss of the PTCH1 gene locus in cardiac fibroma |
| Q35837750 | Medulloblastoma: molecular genetics and animal models |
| Q37319899 | Microphthalmos in association with Gorlin's syndrome |
| Q41489842 | Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11p and 17p in medulloblastomas |
| Q35881960 | Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients |
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| Q34051118 | Molecular insight into medulloblastoma and central nervous system primitive neuroectodermal tumor biology from hereditary syndromes: a review |
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| Q42440116 | Mutational landscape of basal cell carcinomas by whole-exome sequencing. |
| Q24336457 | Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome |
| Q42525885 | Neural variant of fetal rhabdomyoma and naevoid basal cell carcinoma syndrome |
| Q38605389 | Neurocutaneous Syndromes and Brain Tumors |
| Q60843775 | Nevoid Basal Cell Carcinoma (Gorlin) Syndrome |
| Q35231940 | Nevoid Basal cell carcinoma syndrome: a case report and review |
| Q35951367 | Nevoid basal cell carcinoma (Gorlin) syndrome |
| Q72146597 | Nevoid basal cell carcinoma syndrome |
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| Q35830373 | Nevoid basal cell carcinoma syndrome: a review of the literature and a report of a case. |
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| Q42514494 | Nonrandom karyotypic features in basal cell carcinomas of the skin. |
| Q42455481 | Nonrandom numerical chromosome abnormalities in basal cell carcinomas |
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| Q90166275 | Ocular manifestations in Gorlin-Goltz syndrome |
| Q35892074 | Odontogenic Keratocysts in Gorlin-Goltz Syndrome: A Case Report. |
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| Q42490431 | PTCH gene mutations in odontogenic keratocysts |
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| Q35774338 | Patched homologue 1 mutations in four Japanese families with basal cell nevus syndrome |
| Q42458665 | Patching together the genetics of Gorlin syndrome |
| Q41177013 | Per[cyst]ent growth: the odontogenic keratocyst 40 years on. |
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| Q42484281 | Primary cutaneous carcinosarcoma arising in a patient with nevoid basal cell carcinoma syndrome |
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| Q36422767 | The gene for the naevoid basal cell carcinoma syndrome acts as a tumour-suppressor gene in medulloblastoma |
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| Q42528554 | Variable expressivity of patched mutations in flies and humans. |
| Q26782853 | Vismodegib hedgehog-signaling inhibition and treatment of basal cell carcinomas as well as keratocystic odontogenic tumors in Gorlin syndrome |
| Q58585710 | Whole-exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data |
| Q52024661 | [Clinical and genetic study in 22 patients with basal cell nevus syndrome]. |
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