Journal article
Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes
Journal of medical genetics, Vol.24(9), pp.522-524
09/1987
DOI: 10.1136/jmg.24.9.522
PMID: 3118028
Abstract
Genotyping, using plasma proteins or DNA polymorphisms or both, was carried out on 30 families selected through probands with Von Recklinghausen disease. The data provide additional evidence for the exclusion of loci on chromosomes 3 and 5, and chromosome arms 1q, 2p, 4p, 4q, 6q, 7p, 9q, 11p, 11q, and 14q. There was no evidence for genetic heterogeneity at D1S1 (DNF15S2) on chromosome arm 3p, using the Morton test for heterogeneity.
Details
- Title: Subtitle
- Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes
- Creators
- Robert E Ferrell - Department of Biostatistics, University of PittsburghKenneth H Buetow - Fox Chase Cancer CenterJohn K Darby - Stanford University School of MedicineJune E Eichner - Department of Biostatistics, University of PittsburghJeffrey C Murray - University of IowaR Smith - University of IowaMary Waziri - University of IowaSusan Huson - Department of Biostatistics, University of PittsburghVincent M Riccardi - Baylor College of Medicine
- Resource Type
- Journal article
- Publication Details
- Journal of medical genetics, Vol.24(9), pp.522-524
- DOI
- 10.1136/jmg.24.9.522
- PMID
- 3118028
- NLM abbreviation
- J Med Genet
- ISSN
- 0022-2593
- eISSN
- 1468-6244
- Language
- English
- Date published
- 09/1987
- Academic Unit
- Anatomy and Cell Biology; Stead Family Department of Pediatrics; Epidemiology; Pediatric Dentistry; Craniofacial Anomalies Research Center; Dental Research
- Record Identifier
- 9984025319102771