| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0065-230X(08)60871-4 |
| P698 | PubMed publication ID | 8902053 |
| P50 | author | Michael Dean | Q37841464 |
| P2093 | author name string | M Dean | |
| Abirami Chidambaram | |||
| A Chidambaram | |||
| P2860 | cites work | Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome | Q24336457 |
| Mutation and cancer: statistical study of retinoblastoma | Q24618185 | ||
| A comprehensive genetic map of the human genome based on 5,264 microsatellites | Q27860812 | ||
| Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9 | Q28181962 | ||
| Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib. A syndrome | Q28188625 | ||
| Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome | Q28243330 | ||
| Comparative mapping of 50 human chromosome 9 loci in the laboratory mouse | Q28302750 | ||
| The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma | Q35993240 | ||
| Further contribution to the description of phenotypes associated with partial 4q duplication | Q38509026 | ||
| Cutaneous Manifestations of the Proteus Syndrome | Q39297875 | ||
| Nevoid basal-cell carcinoma syndrome | Q39759038 | ||
| Clinical findings in two African-American families with the nevoid basal cell carcinoma syndrome (NBCC). | Q40678896 | ||
| Nevoid basal cell carcinoma syndrome: review of 118 affected individuals | Q40678901 | ||
| Proteus syndrome: clinical evidence for somatic mosaicism and selective review | Q40793429 | ||
| Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11p and 17p in medulloblastomas | Q41489842 | ||
| The basal-cell nevus: its relationship to multiple cutaneous cancers and associated anomalies of development | Q42448276 | ||
| Naevoid basal celled carcinoma associated with a dyskeratosis of the palms and soles. A new entity. | Q42448544 | ||
| HEREDITARY CUTANEMOMANDIBULAR POLYONCOSIS. A SYNDROME OF MYRIAD BASAL-CELL NEVI OF THE SKIN, MANDIBULAR CYSTS, AND INCONSTANT SKELETAL ANOMALIES. | Q42449348 | ||
| Location of gene for Gorlin syndrome | Q42452971 | ||
| Localisation of gene for the naevoid basal-cell carcinoma syndrome | Q42452975 | ||
| Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas | Q42484642 | ||
| Familial nevus sebaceus of Jadassohn: occurrence in three generations. | Q42484759 | ||
| Fine mapping of the locus for nevoid basal cell carcinoma syndrome on chromosome 9q. | Q42495771 | ||
| Chromosome 9 allele loss occurs in both basal and squamous cell carcinomas of the skin | Q42498515 | ||
| Two Cytoplasmic Domains of Mammalian Adenylyl Cyclase Form a G- and Forskolin-activated Enzymein Vitro | Q56535690 | ||
| The nevoid basal cell carcinoma syndrome | Q69666329 | ||
| Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry | Q70732495 | ||
| Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouse | Q71586920 | ||
| Are people who get skin cancer different? | Q72283601 | ||
| Encephalocraniocutaneous lipomatosis, Proteus syndrome, and somatic mosaicism | Q72671835 | ||
| BASAL CELL NEVUS SYNDROME | Q76820879 | ||
| P921 | main subject | nevoid basal cell carcinoma syndrome | Q1536720 |
| P304 | page(s) | 49-61 | |
| P577 | publication date | 1996-01-01 | |
| P1433 | published in | Advances in Cancer Research | Q3113522 |
| P1476 | title | Genetics of the nevoid basal cell carcinoma syndrome | |
| Genetics of the Nevoid Basal Cell Carcinoma Syndrome | |||
| P478 | volume | 70 |
| Q42505133 | Basal cell carcinoma of the eyelid associated with Gorlin-Goltz syndrome |
| Q42439780 | Heterozygous mutations in the tumor suppressor gene PATCHED provoke basal cell carcinoma-like features in human organotypic skin cultures |
| Q21203684 | Histogenesis of retinal dysplasia in trisomy 13 |
| Q24532233 | TTF-2, a new forkhead protein, shows a temporal expression in the developing thyroid which is consistent with a role in controlling the onset of differentiation |
| Q33933775 | UV-specific mutations of the human patched gene in basal cell carcinomas from normal individuals and xeroderma pigmentosum patients |
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