Localization of a locus for Charcot-Marie-Tooth neuropathy type la (CMT1A) to chromosome 17

Molecular Cloning: A Laboratory Manual

2001 • 133,517 citations

THE CLINICAL FEATURES OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPES I AND II

1980 • 805 citations

Report of the committee on the genetic constitution of the X chromosome (Part 1 of 3)

1990 • 597 citations

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1984 • 586 citations

Lower Motor and Primary Sensory Neuron Diseases With Peroneal Muscular Atrophy

1968 • 560 citations

The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

1956 • 434 citations

Report of the committee on methods of linkage analysis and reporting

1985 • 325 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

Multigene Family for Sarcomeric Myosin Heavy Chain in Mouse and Human DNA: Localization on a Single Chromosome

1983 • 141 citations

Hereditary motor and sensory polyneuropathy (peroneal muscular atrophy)*

1974 • 88 citations

PvuII RFLP inside the human estrogen receptor gene

1987 • 78 citations

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

1983 • 76 citations

The human thyroglobulin gene: A polymorphic marker localized distal to C-MYC on chromosome 8 band q24

1985 • 76 citations

Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.

1983 • 74 citations

Report of the committee on the genetic constitution of chromosome 1

1990 • 70 citations

Localization of a human heat-shock HSP 70 gene sequence to chromosome 6 and detection of two other loci by somatic-cell hybrid and restriction fragment length polymorphism analysis

1987 • 66 citations

Report of the nomenclature committee and the 1989 catalog of mapped genes (Part 1 of 3)

1989 • 63 citations

The 1991 catalog of mapped genes and report of the nomenclature committee (Part 1 of 5)

1991 • 62 citations

Report of the committee on the genetic constitution of chromosomes 17, 18 and 19

1985 • 60 citations

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

1978 • 55 citations

Polymorphism of immunoglobulin lambda constant region genes in populations from France, Lebanon and Tunisia.

1988 • 51 citations

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

1983 • 50 citations

Three RFLPs are detected by an alpha spectrin genomic clone

1987 • 41 citations

Report of the committee on the genetic constitution of chromosome 1

1989 • 39 citations

The human myelin-basic-protein gene: chromosomal localization and RFLP analysis.

1987 • 38 citations

Case of Progressive Neural Muscular Atrophy (Peroneal or Charcot-Marie-Tooth Type) in Which the Upper Limbs are also Affected

1924 • 34 citations

A DNA polymorphism of the apoprotein AII gene in hypertriglyceridaemia

1986 • 25 citations

Evidence for linkage of type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1

1982 • 25 citations

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

1988 • 25 citations

A linkage group of five DNA markers on human chromosome 10

1988 • 23 citations

Assignment of tissue-type plasminogen activator to chromosome 8 in man and identification of a common restriction length polymorphism within the gene.

1984 • 23 citations

Extension of human acid α‐glucosidase polymorphism by isoelectric focusing in polyacrylamide gel

1982 • 21 citations

A revised map of chromosome 1

1984 • 21 citations

EcoRI RFLP linked to the humanmybgene

1986 • 19 citations

Hereditary chronic polyneuropathy

1969 • 18 citations

BanII and ScaI RFLPs at the human p53 gene locus

1988 • 16 citations

A DNA marker for human chromosome 8 that detects alleles of differing sizes

1986 • 16 citations

Segregation patterns of polymorphic restriction sites of the gene encoding the alpha subunit of human chorionic gonadotropin in trophoblastic disease.

1984 • 16 citations

Genetic linkage relationships of Charcot‐Marie‐Tooth disease (HMSN‐Ib) to chromosome 1 markers

1987 • 14 citations

RFLP for the human pepsinogen C gene (PGC)

1988 • 14 citations

LINKAGE STUDY BETWEEN THE AMYLOID GENE AND FAMILIAL ALZHEIMERS-DISEASE

1987 • 12 citations

Abstracts of workshop presentations (Part 12 of 13)

1985 • 12 citations

Centromeric linkage in man

1975 • 12 citations

Linkage analysis of Charcot-Marie-Tooth neuropathy (HMSN type I)

1987 • 10 citations

A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37.

1986 • 9 citations

Another elliptocytosis locus on chromosome 1?

1979 • 8 citations

Two RFLPs identified by a human chromosome #2 clone at 2p15–2p16 (HGM8 assignment no. D2S5)

1985 • 8 citations

Linkage between the loci for peptidase D and apolipoprotein CII on chromosome 19

1985 • 4 citations

Human TaqI RFLP recognized by neurofilament gene probes

1988 • 3 citations

Deleted Work

1955 • 0 citations