| scholarly article | Q13442814 |
| P2093 | author name string | D H Ledbetter | |
| A G Menon | |||
| P O'Connell | |||
| M R Wallace | |||
| R L White | |||
| J W Fountain | |||
| D C Rich | |||
| R E Fournier | |||
| R J Leach | |||
| A M Brereton | |||
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| The William Allan Memorial Award address: Reverse genetics and beyond | Q35200050 | ||
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| Multipoint linkage analysis in neurofibromatosis type I: an international collaboration | Q35247369 | ||
| Fine structure DNA mapping studies of the chromosomal region harboring the genetic defect in neurofibromatosis type I. | Q35550484 | ||
| Isolation of a cDNA clone encoding pancreatic polypeptide | Q36486481 | ||
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| Transforming genes of carcinomas and neuroblastomas introduced into mouse fibroblasts | Q42801594 | ||
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| Linkage studies with chromosome 17 DNA markers in 45 neurofibromatosis 1 families | Q46640982 | ||
| Similarity of protein encoded by the human c-erb-B-2 gene to epidermal growth factor receptor | Q48369441 | ||
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| Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17 | Q56439564 | ||
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| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 58-67 | |
| P577 | publication date | 1989-01-01 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17. | |
| P478 | volume | 44 |
| Q72567865 | A de novo nonsense mutation in exon 28 of the neurofibromatosis type 1 (NF1) gene |
| Q35247285 | A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene |
| Q35198336 | Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12. |
| Q35364327 | Comparative map for mice and humans |
| Q67871559 | Comparative map for mice and humans |
| Q35867180 | Direct construction of a chromosome-specific NotI linking library from flow-sorted chromosomes |
| Q35550484 | Fine structure DNA mapping studies of the chromosomal region harboring the genetic defect in neurofibromatosis type I. |
| Q35247407 | Genetic analysis of eight loci tightly linked to neurofibromatosis 1 |
| Q37286548 | Homozygous deletions within human chromosome band 9p21 in melanoma |
| Q35895599 | In vitro modeling of hyperpigmentation associated to neurofibromatosis type 1 using melanocytes derived from human embryonic stem cells |
| Q33594500 | Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphism |
| Q35195848 | Localization of DNA sequences to a region within Xp11.21 between incontinentia pigmenti (IP1) X-chromosomal translocation breakpoints |
| Q34022409 | Mast cells and the neurofibroma microenvironment |
| Q35247369 | Multipoint linkage analysis in neurofibromatosis type I: an international collaboration |
| Q36960893 | Pathogenesis of plexiform neurofibroma: tumor-stromal/hematopoietic interactions in tumor progression |
| Q35939735 | Peripheral nerve tumors: management strategies and molecular insights |
| Q35247332 | Precise localization of NF1 to 17q11.2 by balanced translocation |
| Q67513370 | Preferential mutation of the neurofibromatosis type 1 gene in paternally derived chromosomes |
| Q35197416 | Refined physical and genetic mapping of the NF1 region on chromosome 17 |
| Q30501214 | The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focus |
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