Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1983 • 26,063 citations

A simple salting out procedure for extracting DNA from human nucleated cells

1988 • 20,341 citations

Sequential tests for the detection of linkage.

1955 • 1,590 citations

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

1985 • 1,207 citations

Genetic and clinical aspects of Charcot‐Marie‐Tooth's disease

1974 • 874 citations

Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17

1987 • 691 citations

Lower Motor and Primary Sensory Neuron Diseases With Peroneal Muscular Atrophy

1968 • 560 citations

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

1986 • 468 citations

Interstitial deletion of (17)(p11.2p11.2) in nine patients

1986 • 387 citations

Use of cyclosporin a in establishing epstein-barr virus-transformed human lymphoblastoid cell lines

1984 • 355 citations

Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1.

1982 • 220 citations

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17

1989 • 198 citations

Regional mapping panel for human chromosome 17: Application to neurofibromatosis type 1

1987 • 120 citations

Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome.

1988 • 92 citations

Genetic linkage evidence for heterogeneity in Charcot‐Marie‐Tooth neuropathy (HMSN type I)

1983 • 76 citations

[5] Precipitation of nucleic acids

1987 • 75 citations

Human chromosomal assignments for 14 argininosuccinate synthetase pseudogenes: cloned DNAs as reagents for cytogenetic analysis.

1984 • 66 citations

Fine structure DNA mapping studies of the chromosomal region harboring the genetic defect in neurofibromatosis type I.

1989 • 63 citations

Variability of human linkage data.

1978 • 58 citations

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

1987 • 55 citations

Charcot‐Marie‐Tooth disease: Data for genetic counseling relating age to risk

1978 • 55 citations

Linkage evidence for genetic heterogeneity among kinships with hereditary motor and sensory neuropathy, type I.

1983 • 50 citations

Localization of X-Linked Dominant Charcot-Marie-Tooth Disease (CMT 2) to Xq13

1986 • 45 citations

Linkage of autosomal dominant type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1.

1982 • 41 citations

Direct construction of a chromosome-specificNotI linking library from flow-sorted chromosomes

1989 • 41 citations

Linkage studies with chromosome 17 DNA markers in 45 neurofibromatosis 1 families

1987 • 31 citations

Chromosome I linkage studies in Charcot-Marie-Tooth neuropathy type I.

1988 • 25 citations

Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markers

1989 • 12 citations

Absence of linkage with the Duffy blood group in a family with Charcot-Marie-Tooth neuropathy

1988 • 10 citations