(Q35245493)

7 August 2017

title

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

1 reference

7 August 2017

Griffiths LR

1

1 reference

7 August 2017

Zwi MB

series ordinal

2

1 reference

7 August 2017

McLeod JG

series ordinal

3

1 reference

7 August 2017

Nicholson GA

series ordinal

4

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 May 1988

1 reference

American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

42

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7 August 2017

issue

5

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7 August 2017

page(s)

756-771

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

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

Isolation and sequence characterization of a cDNA clone of human antithrombin III

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

Primary structure of the human renin gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

A polymorphic DNA marker genetically linked to Huntington's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

Probable Genetic Linkage between Human Serum Amylase (Amy2) and Duffy Blood Group

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

Two RFLPs at the human renin (ren) gene locus

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

A discordant sibship analysis between beta-NGF and neurofibromatosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

Detection of specific sequences among DNA fragments separated by gel electrophoresis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

A general method for isolation of high molecular weight DNA from eukaryotes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

Confirmation of genetic heterogeneity in autosomal dominant forms of congenital cataracts from linkage studies

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

Isolation of a cDNA clone for human antithrombin III

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

Probable assignment of the Duffy blood group locus to chromosome 1 in man

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

Molecular genetic evidence for heterogeneity in manic depression.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715168

The linkage and mapping relationships of 1 qh

26 September 2018

1 reference

12 December 2020

Four further families informative for 1q and the Duffy blood group

1 reference

12 December 2020

Confirmation of linkage between antithrombin III and Duffy blood group and assignment of AT3 to 1q22 lead to q25

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

Assignment of the human antithrombin III structural gene to chromosome 1q23-25

1 reference

12 December 2020

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs

1 reference

12 December 2020

Linkage relationships of the gene for the beta subunit of nerve growth factor (NGFB) with other chromosome 1 marker loci

1 reference

12 December 2020

X-linked neuropathy: gene localization with DNA probes

1 reference

12 December 2020

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

1 reference

12 December 2020

Regional chromosomal assignment of human renin gene to 1q12→qter and use in linkage studies in Charcot-Marie-Tooth disease

1 reference

12 December 2020

Identifiers

PMC publication ID

1715168

1 reference

7 August 2017

1 reference