The Autosomal Recessive Form of CMT Disease Linked to 5q31‐q33

A comprehensive genetic map of the human genome based on 5,264 microsatellites

Colette Dib, Sabine Fauré, Cécile Fizames et al. · Nature · 1996 · 3K citations

Genetic Analysis, Haplotype Determination, Medicine +10

Disruption of the murine homeobox gene Cdx1 affects axial skeletal identities by altering the mesodermal expression domains of Hox genes

Vasanta Subramanian, Barbara I. Meyer · Cell · 1995 · 350 citations · Full text

Developmental Biology, Bone Morphogenic Protein, Mesodermal Expression Domains +7

Molecular cloning, sequencing and expression of the mRNA encoding human Cdx1 and Cdx2 homeobox. Down-regulation of Cdx1 and Cdx2 mRNA expression during colorectal carcinogenesis

Gustavo V. Mallo, Hocine Rechreche, Jean‐Marc Frigério et al. · International Journal of Cancer · 1997 · 205 citations

Pathology, Cancer Biology, Tumor Biology +17

Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24

Luba Kalaydjieva, Joachim Hallmayer, David Chandler et al. · Nature Genetics · 1996 · 185 citations

Peripheral Nerves, Neurogenomics, Novel Demyelinating Neuropathy +11

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q

Kamel Ben Othmane, F. Hentatl, Felicia Lennon et al. · Human Molecular Genetics · 1993 · 177 citations