Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in dutch families
Authors:
- Wilma BergmanWBWilma Bergman
- Marcel R. NelenMNMarcel R. Nelen
- Ellien van der Kooij-MeijsEKEllien van der Kooij-Meijs
- Iems HendrikseIHIems Hendrikse
- Juul Th. WijnenJWJuul Th. Wijnen
- Paul Meera KhanPKPaul Meera Khan
- Eduard C. KlasenEKEduard C. Klasen
- Rune R. FrantsRFRune R. Frants
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- A hypervariable repeated sequence on human chromosome 1p36Human Genetics, 1987
- Exclusion mapping.Journal of Medical Genetics, 1987
- Variable Number of Tandem Repeat (VNTR) Markers for Human Gene MappingScience, 1987
- Report of the committee on the genetic constitution of chromosomes 1 and 2Cytogenetic and Genome Research, 1987
- Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophyHuman Genetics, 1985
- The human thyroglobulin gene contains two 15-17 kb introns near its 3′-endNucleic Acids Research, 1983
- The dysplastic nevus syndrome Our definitionThe American Journal of Dermatopathology, 1982
- The Rising Incidence and Mortality Rate of Malignant MelanomaThe Journal of Dermatologic Surgery and Oncology, 1982
- Familial atypical multiple mole-melanoma syndrome.Journal of Medical Genetics, 1978
- Origin of familial malignant melanomas from heritable melanocytic lesions. 'The B-K mole syndrome'Archives of Dermatology, 1978