Etiological heterogeneity in X-linked spastic paraplegia (Q35199527)

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Language	Label	Description	Also known as
English	Etiological heterogeneity in X-linked spastic paraplegia	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

3479019

retrieved

7 August 2017

title

Etiological heterogeneity in X-linked spastic paraplegia (English)

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stated in

Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

main subject

heterogeneity

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based on heuristic

inferred from title

author

Mark Lathrop

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6

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Lathrop M

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

Jean-Marc Lalouel

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7

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Lalouel JM

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

author name string

Keppen LD

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1

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

Leppert MF

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2

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

O'Connell P

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3

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

Nakamura Y

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4

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

Stauffer D

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5

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

White R

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8

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

language of work or name

English

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publication date

1 November 1987

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

published in

American Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

volume

41

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

issue

5

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Europe PubMed Central

PubMed publication ID

3479019

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7 August 2017

page(s)

933-943

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PubMed publication ID

3479019

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7 August 2017

cites work

A sex-linked recessive form of spastic paraplegia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

retrieved

28 July 2018

Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

retrieved

28 July 2018

Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

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28 July 2018

The genetic linkage map of the human X chromosome

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

retrieved

28 July 2018

Rapid transfer of DNA from agarose gels to nylon membranes

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

retrieved

28 July 2018

Linkage studies of X-linked recessive spastic paraplegia using DNA probes.

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

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28 July 2018

Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study.

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

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28 July 2018

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

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28 July 2018

X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

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28 July 2018

Strumpell's pure familial spastic paraplegia: case study and review of the literature

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

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28 July 2018

Strategies for multilocus linkage analysis in humans

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

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26 September 2018

Easy calculations of lod scores and genetic risks on small computers

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

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26 September 2018

Hereditary cerebral palsy; a preliminary report

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684330

retrieved

15 November 2018

Sex-linked spastic paraplegia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3479019

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3479019

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3479019

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two kindreds with a sex-linked recessive form of spastic paraplegia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3479019

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1684330

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3479019

retrieved

7 August 2017

PubMed publication ID

3479019

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3479019

retrieved

7 August 2017

 

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