(Q35202259)

7 August 2017

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

1 reference

7 August 2017

T D Bird

1

1 reference

7 August 2017

J Ott

series ordinal

2

1 reference

7 August 2017

E R Giblett

series ordinal

3

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 May 1982

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

34

1 reference

7 August 2017

388-394

1 reference

7 August 2017

3

1 reference

Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685353

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685353

Naevoid basal cell carcinoma syndrome and Charcot-Marie-Tooth disease: two autosomal dominant disorders segregating in a family

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685353

Charcot-Marie-Tooth disease: data for genetic counseling relating age to risk

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685353

Genetic evidence for four common alleles at the phosphoglucomutase-1 locus (PGM1) detectable by isoelectric focusing

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685353

A maximum likelihood map of chromosome 1

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685353

Linkage studies in spinocerebellar ataxia (SCA)

13 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6952764

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6952764

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMCID

1685353

1 reference

7 August 2017

1 reference