A Duplication in Chromosome 4q35 Is Associated with Hereditary Benign Intraepithelial Dyskeratosis

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

Peter Raeymaekers, Vincent Timmerman, Eva Nelis et al. · Neuromuscular Disorders · 1991 · 598 citations

Mendelian Disorder, Genetic Disorder, Genetics +6

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set–recoding and fuzzy inheritance

Jeffrey R. O’Connell, Daniel E. Weeks · Nature Genetics · 1995 · 503 citations

Genetic Analysis, Linkage Disequilibrium, Genotype Set–recoding +13

The fat tumor suppressor gene in Drosophila encodes a novel member of the cadherin gene superfamily

Paul A. Mahoney, Ursula Weber, Patricia Leigh. Onofrechuk et al. · Cell · 1991 · 456 citations

Developmental Biology, Signaling Pathway, Cadherin Gene +6

The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication

Vincent Timmerman, Eva Nelis, Wim Van Hul et al. · Nature Genetics · 1992 · 391 citations

Neurodegenerative Diseases, Peripheral Nerves, Genetic Disorder +8

Molecular Cloning and Tissue Expression ofFAT,the Human Homologue of theDrosophila fatGene That Is Located on Chromosome 4q34–q35 and Encodes a Putative Adhesion Molecule

Jenny Dunne, Andrew M. Hanby, Richard Poulsom et al. · Genomics · 1995 · 165 citations

Developmental Genetics, Genetics, Natural Sciences +9