Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor
- 30 June 1990
- Vol. 7 (3) , 434-438
- https://doi.org/10.1016/0888-7543(90)90179-x
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
- A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndromeGenomics, 1989
- Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinomaHuman Genetics, 1989
- Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11Cell, 1988
- Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13Nature, 1988
- Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11Nature, 1988
- Genetic Origin of Mutations Predisposing to RetinoblastomaScience, 1985
- DNA polymorphism and molecular pathology of the human globin gene clustersHuman Genetics, 1985
- Expression of recessive alleles by chromosomal mechanisms in retinoblastomaNature, 1983
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983
- Cloning and characterization of five overlapping cDNAs specific for the human proα 1(I) collagen chainNucleic Acids Research, 1982