Gene for topoisomerase III maps within the Smith-Magenis syndrome critical region: Analysis of cell-cycle distribution and radiation sensitivity

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

1995 • 1,197 citations

Flow cytometric measurement of total DNA content and incorporated bromodeoxyuridine.

1983 • 978 citations

The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase.

1994 • 686 citations

The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1A

1992 • 497 citations

Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

1991 • 342 citations

Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)

1996 • 319 citations

A Revision of the Lissencephaly and Miller-Dieker Syndrome Critical Regions in Chromosome 17p13.3

1997 • 194 citations

Identification of the yeast TOP3 gene product as a single strand-specific DNA topoisomerase.

1992 • 127 citations

Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients.

1996 • 126 citations

Human TOP3: a single-copy gene encoding DNA topoisomerase III.

1996 • 125 citations

Testing the Role of p53 in the Expression of Genetic Instability and Apoptosis in Ataxia-telangiectasia

1994 • 101 citations

Clinical, cytogenetic, and molecular evidence for an infant with Smith–Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion

1993 • 89 citations

The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2.

1995 • 69 citations

Expression cloning of multiple human cDNAs that complement the phenotypic defects of ataxia-telangiectasia group D fibroblasts.

1993 • 68 citations

A genetic map of human chromosome 17p

1990 • 68 citations

The Smith-Magenis syndrome [del(17)p11.2]: Clinical review and molecular advances

1996 • 59 citations

Genetic analysis of NF1: Identification of close flanking markers on chromosome 17

1987 • 55 citations

Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients

1996 • 52 citations

Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p

1992 • 40 citations

Effects of yeast DNA topoisomerase III on telomere structure.

1995 • 39 citations

Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome.

1995 • 37 citations

Overexpression of a truncated human topoisomerase III partially corrects multiple aspects of the ataxia-telangiectasia phenotype

1997 • 35 citations

Physical Mapping of Chromosome 17 Cosmids by Fluorescence in Situ Hybridization and Digital Image Analysis

1994 • 33 citations

Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybrids.

1990 • 30 citations