Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc? receptor gene region (Q41659080)

reason for preferred rank

6 October 2017

title

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc? receptor gene region (English)

1 reference

28 October 2022

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene region (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1683643

28 October 2022

1 reference

28 October 2022

8

M. C. King

1 reference

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28 October 2022

author name string

R. V. Lebo

1

1 reference

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28 October 2022

P. F. Chance

2

1 reference

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28 October 2022

P. J. Dyck

3

1 reference

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28 October 2022

M. T. Redila-Flores

4

1 reference

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28 October 2022

E. D. Lynch

5

1 reference

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28 October 2022

M. S. Golbus

6

1 reference

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28 October 2022

T. D. Bird

7

1 reference

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28 October 2022

L. A. Anderson

9

1 reference

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28 October 2022

J. Hall

10

1 reference

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28 October 2022

publication date

1 November 1991

1 reference

6 October 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1683643

http://link.springer.com/content/pdf/10.1007/BF00204921.pdf

28 October 2022

work available at URL

1 reference

http://link.springer.com/article/10.1007/BF00204921/fulltext.html

28 October 2022

1 reference

http://link.springer.com/content/pdf/10.1007/BF00204921

28 October 2022

1 reference

28 October 2022

1 reference

6 October 2017

volume

88

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6 October 2017

issue

1

1 reference

6 October 2017

page(s)

1-12

1 reference

Construction of human chromosome-specific DNA libraries from flow-sorted chromosomes

6 October 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00204921

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00204921

Complex partial status epilepticus of extratemporal origin: report of a case

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00204921

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

21 January 2018

1 reference

12 December 2020

NIH Conference: Immunoglobulin G Fc receptor-mediated clearance in autoimmune diseases

1 reference

12 December 2020

Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13

1 reference

12 December 2020

The polymorphic Fc gamma receptor II gene maps to human chromosome 1q.

1 reference

12 December 2020

The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1.

1 reference

12 December 2020

Tissue-specific and developmental regulation of rat Na,K-ATPase catalytic alpha isoform and beta subunit mRNAs.

1 reference

12 December 2020

Twenty-eight loci form a continuous linkage map of markers for human chromosome 1.

1 reference

12 December 2020

Strategies for multilocus linkage analysis in humans

1 reference

12 December 2020

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

1 reference

12 December 2020

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations

1 reference

12 December 2020

Rare McArdle disease locus polymorphic site on 11q13 contains CpG sequence

1 reference

12 December 2020

Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family

1 reference

12 December 2020

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Demonstration of Fc gamma receptors on human peripheral nerve fibres

1 reference

12 December 2020

LIPIN: an interactive data entry and management program for LIPED.

1 reference

12 December 2020

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

1 reference

12 December 2020

Organization of the human and mouse low-affinity Fc gamma R genes: duplication and recombination

1 reference

12 December 2020

Longitudinal study of neuropathic deficits and nerve conduction abnormalities in hereditary motor and sensory neuropathy type 1

1 reference

12 December 2020

Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17

1 reference

12 December 2020

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

1 reference

12 December 2020

Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood

1 reference

12 December 2020

Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).

1 reference

12 December 2020

X-linked neuropathy: gene localization with DNA probes

1 reference

12 December 2020

X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

1 reference

12 December 2020

Gene mapping with sorted chromosomes

1 reference

12 December 2020

Peripheral neuropathy and anti-MAG antibodies

1 reference

12 December 2020

Characterization of the human Na,K-ATPase alpha 2 gene and identification of intragenic restriction fragment length polymorphisms

1 reference

12 December 2020

Human placental Na+,K+-ATPase alpha subunit: cDNA cloning, tissue expression, DNA polymorphism, and chromosomal localization

1 reference

12 December 2020

Genetic aspects of hereditary motor and sensory neuropathy (types I and II)

1 reference

12 December 2020

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

1 reference

12 December 2020

1 New bacteriophage lambda vectors with positive selection for cloned insects

1 reference

12 December 2020

Flow-sorting analysis of normal and abnormal human genomes

1 reference

12 December 2020

Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers

1 reference

12 December 2020

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

1 reference

12 December 2020

Chromosomal localization of human Na+, K+-ATPase alpha- and beta-subunit genes

1 reference

12 December 2020

Cytogenetics and Cell Genetics

2

51

951

LA Anderson

1989

1 reference

A genetic linkage map of the human genome

28 October 2022

14

1 reference

28 October 2022

Mayo Clinic Proceedings

18

58

430

PJ Dyck

1983

1 reference

28 October 2022

Identifiers

DOI

10.1007/BF00204921

1 reference

Dimensions publication ID

6 October 2017

1038843750

0 references

1 reference