(Q73075233)

English

Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2

scientific article published on 01 February 1997

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scholarly article

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1 November 2019

Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2 (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9034002%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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based on heuristic

inferred from title

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based on heuristic

inferred from title

spastic paraparesis

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based on heuristic

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author name string

W H Raskind

1

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1 November 2019

M A Pericak-Vance

2

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1 November 2019

F Lennon

3

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J Wolff

4

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1 November 2019

H P Lipe

5

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1 November 2019

T D Bird

6

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publication date

1 February 1997

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1 November 2019

American Journal of Medical Genetics Part A

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1 November 2019

74

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1 November 2019

1

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26-36

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1 November 2019

Strümpell's familial spastic paraplegia: genetics and neuropathology

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

1 reference

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21 January 2018

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group

1 reference

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21 January 2018

Developmental trends of sleep-disordered breathing in Prader-Willi syndrome: the role of obesity

1 reference

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21 January 2018

Classification of the hereditary ataxias and paraplegias

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene

1 reference

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21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

Avoiding recomputation in linkage analysis.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

Simple tandem DNA repeats and human genetic disease

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970221%2974%3A1%3C26%3A%3AAID-AJMG7%3E3.0.CO%3B2-T

21 January 2018

Identifiers

10.1002/(SICI)1096-8628(19970221)74:1<26::AID-AJMG7>3.0.CO;2-T

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9034002%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9034002%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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