Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus
Human Genetics1991Vol. 87(2), pp. 207–210
Citations Over TimeTop 10% of 1991 papers
G.M. Glenn, Lambert N. Daniel, Peter Choyke, W. Marston Linehan, Edward H. Oldfield, Michael B. Gorin, Shigeto Hosoe, Farida Latif, Gary H. Weiss, McClellan M. Walther, Michael I. Lerman, Berton Zbar
Related Papers
- → GENETIC EVIDENCE FOR A SILENT SUC GENE IN YEAST(1981)38 cited
- → Mutation in the STR Locus D21S11 of Father Causing Allele Mismatch in the Child(2004)14 cited
- → Structural polymorphisms at the X-chromosomal short tandem repeat loci DXS10134, DXS10135, DXS10146 and DXS10148(2011)1 cited
- → The human D11S554 locus: four distinct families of repeat pattern alleles at one locus(1993)27 cited
- → HIGH RESOLUTION RECOMBINATION ANALYSIS OF THE PYRIDOXINE-1 LOCUS OFNEUROSPORA(1968)7 cited