| scholarly article | Q13442814 |
| P50 | author | James F. Gusella | Q1602688 |
| Guy A. Rouleau | Q3121500 | ||
| Jonathan L Haines | Q73570557 | ||
| P2093 | author name string | B R Seizinger | |
| R L Martuza | |||
| W Wertelecki | |||
| D W Superneau | |||
| P2860 | cites work | Strategies for multilocus linkage analysis in humans | Q27860521 |
| Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22 | Q28265748 | ||
| Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresis | Q28267117 | ||
| Human chromosome 22. | Q30495423 | ||
| Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma | Q30502386 | ||
| Molecular genetic approach to human meningioma: loss of genes on chromosome 22 | Q30502412 | ||
| Expression of recessive alleles by chromosomal mechanisms in retinoblastoma | Q34264957 | ||
| Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis | Q34685520 | ||
| Neurofibromatosis 2: clinical and DNA linkage studies of a large kindred | Q34685814 | ||
| A linkage and physical map of chromosome 22, and some applications to gene mapping | Q35246088 | ||
| A genetic linkage map of the long arm of human chromosome 22. | Q35551356 | ||
| Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors | Q36426834 | ||
| Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma | Q39590706 | ||
| Neurofibromatosis 2 (bilateral acoustic neurofibromatosis). | Q39600883 | ||
| Von Recklinghausen neurofibromatosis | Q40262766 | ||
| An anonymous single copy chromosome 22 clone, D22S10 (22c1-18) identifies an RFLP with PstI. | Q40472072 | ||
| RFLP detected with a 5'-bcr-gene-sequence (HGM8 provisional no. D22S11). | Q40565493 | ||
| A computer program for linkage analysis of general human pedigrees | Q43144003 | ||
| Loss of genes on the long arm of chromosome 22 in human meningiomas | Q44363728 | ||
| Loss of constitutional heterozygosity in colon carcinoma from patients with familial polyposis coli. | Q54754246 | ||
| Chromosome translocation t(14;22) and oncogene (c-sis) variant in a pedigree with familial meningioma | Q55670485 | ||
| Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22 | Q59076230 | ||
| Genetic linkage map of human chromosome 21 | Q69930146 | ||
| Restriction sites containing CpG show a higher frequency of polymorphism in human DNA | Q72722161 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | neurofibromatosis type II | Q1935832 |
| P304 | page(s) | 323-328 | |
| P577 | publication date | 1990-02-01 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22. | |
| P478 | volume | 46 |
| Q30501644 | A t(4;22) in a meningioma points to the localization of a putative tumor-suppressor gene |
| Q30541671 | Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors |
| Q30495388 | Constitutional ring chromosomes and tumour suppressor genes |
| Q55037406 | Deletion mapping of chromosome 1p and 22q in pheochromocytoma. |
| Q55483500 | Familial CNS tumors |
| Q30502716 | Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas |
| Q37828436 | Gene expression profiling of meningiomas: current status after a decade of microarray-based transcriptomic studies |
| Q36941609 | Genetic alterations in glioma and medulloblastoma |
| Q40531104 | Genetic alterations of brain tumors |
| Q57813524 | Identification of twelve new RFLP-markers on chromosome 22q11-qter |
| Q36721514 | Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome |
| Q94395801 | La lutte contre la neurofibromatose: Mémorandum d'une réunion conjointe OMS/NNFF |
| Q30495393 | Molecular genetics of neurological tumours |
| Q30449267 | Neurofibromatosis: chronological history and current issues |
| Q48674799 | Pediatric neurofibromatosis type 2: clinical and molecular presentation, management of vestibular schwannomas, and hearing rehabilitation |
| Q68146571 | Prevention and control of neurofibromatosis: memorandum from a joint WHO/NNFF meeting |
| Q71131047 | Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas |
| Q72573384 | Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas |
| Q55482841 | Successful treatment for a metastatic supratentorial malignant rhabdoid tumor. |
| Q24678711 | The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin |
| Q30499489 | Tumor-suppressor genes: cardinal factors in inherited predisposition to human cancers |
| Q30502816 | Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease |
| Q38264266 | Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review |
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