N.J. Barton

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.

Andrew O.M. Wilkie, Veronica J. Buckle, Peter C. Harris et al. · PubMed · 1990 · 135 citations

DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASE

Janette Lamb, P.C. Harris, R H Lindenbaum et al. · The Lancet · 1989 · 84 citations

Chromatin, Genome Instability, Genetic Disorder +9

The gene for autosomal dominant polycystic kidney disease lies in a 750-kb CpG-rich region

Gregory G. Germino, Debra Weinstat‐Saslow, Heinz Himmelbauer et al. · Genomics · 1992 · 83 citations

Mendelian Disorder, Genetic Disorder, Medicine +12

Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16.

Gregory G. Germino, N.J. Barton, Janette Lamb et al. · PubMed · 1990 · 68 citations

Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1).

A Snarey, Spencer A. Thomas, Michael Schneider et al. · PubMed · 1994 · 59 citations