Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q (Q24672217): Difference between revisions

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label / astlabel / ast
 
Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q
description / hydescription / hy
գիտական հոդված
1995 թվականի հունվարին հրատարակված գիտական հոդված
description / astdescription / ast
artículu científicu
artículu científicu espublizáu en 1995
description / pt-brdescription / pt-br
artigo científico
artigo científico (publicado na 1995)
description / ukdescription / uk
наукова стаття
наукова стаття, опублікована в січні 1995
description / urdescription / ur
 
سائنسی مضمون
description / fadescription / fa
 
مقالهٔ علمی
description / bndescription / bn
 
১৯৯৫-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ
description / hywdescription / hyw
 
1995 թուականի Յունուարին հրատարակուած գիտական յօդուած
Property / original language of film or TV show
 
Property / original language of film or TV show: English / rank
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Property / PubMed publication ID
 
Property / PubMed publication ID: 7625443 / rank
 
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Property / PubMed publication ID: 7625443 / qualifier
 
Property / cites work
 
Property / cites work: Hereditary (familial) spastic paraplegia; further clinical and pathologic observations. / rank
 
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Property / cites work: Hereditary (familial) spastic paraplegia; further clinical and pathologic observations. / 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=1801321
retrieved: 28 September 2017
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Property / cites work
 
Property / cites work: Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q. / rank
 
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Property / cites work: Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q. / 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=1801321
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Property / cites work
 
Property / cites work: Hereditary "pure" spastic paraplegia: a study of nine families / rank
 
Normal rank
Property / cites work: Hereditary "pure" spastic paraplegia: a study of nine families / 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=1801321
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Property / cites work
 
Property / cites work: Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families / rank
 
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Property / cites work: Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families / 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=1801321
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Property / cites work
 
Property / cites work: Etiological heterogeneity in X-linked spastic paraplegia / rank
 
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Property / cites work: Etiological heterogeneity in X-linked spastic paraplegia / 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=1801321
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Property / cites work
 
Property / cites work: A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease). / rank
 
Normal rank
Property / cites work: A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease). / 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=1801321
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Property / cites work
 
Property / cites work: Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p / rank
 
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Property / cites work: Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p / 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=1801321
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Property / cites work: A second-generation linkage map of the human genome / rank
 
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Property / cites work: A second-generation linkage map of the human genome / 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=1801321
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Property / cites work: Strumpell's pure familial spastic paraplegia: case study and review of the literature / rank
 
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Property / cites work: Strumpell's pure familial spastic paraplegia: case study and review of the literature / reference
 
stated in: PubMed Central
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Property / cites work: Hereditary spastic paraplegia in Western Norway. / rank
 
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Property / cites work: Hereditary spastic paraplegia in Western Norway. / reference
 
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Property / cites work: Linkage studies of X-linked recessive spastic paraplegia using DNA probes. / rank
 
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Property / cites work: Linkage studies of X-linked recessive spastic paraplegia using DNA probes. / reference
 
Property / cites work
 
Property / cites work: HEREDITARY SPASTIC PARAPLEGIA. / rank
 
Normal rank
Property / cites work: HEREDITARY SPASTIC PARAPLEGIA. / 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=1801321
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Property / cites work: Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene / rank
 
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Property / cites work: Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene / 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=1801321
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Property / cites work: Hereditary spastic paraplegia with neurogenic bladder disturbances and syndactylia / rank
 
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Property / cites work: Hereditary spastic paraplegia with neurogenic bladder disturbances and syndactylia / 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=1801321
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Property / cites work: The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigree / rank
 
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Property / cites work: The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigree / reference
 
stated in: PubMed
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Property / cites work: DNA duplication associated with Charcot-Marie-Tooth disease type 1A / rank
 
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stated in: PubMed
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Property / cites work: The phenotype of "pure" autosomal dominant spastic paraplegia / rank
 
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stated in: PubMed
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Property / cites work: Sphincter involvement in hereditary spastic paraplegia / rank
 
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Property / cites work: Sphincter involvement in hereditary spastic paraplegia / reference
 
stated in: PubMed
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Property / cites work: Sleep-associated breathing disorders in morbidly obese children and adolescents / rank
 
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stated in: Crossref
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Latest revision as of 21:56, 7 August 2021

scientific article
Language Label Description Also known as
English
Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q
scientific article

    Statements

    title
    Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q (English)
    0 references
    author name string
    J K Fink
    series ordinal
    1
    0 references
    C T Wu
    series ordinal
    2
    0 references
    S M Jones
    series ordinal
    3
    0 references
    G B Sharp
    series ordinal
    4
    0 references
    B M Lange
    series ordinal
    5
    0 references
    A Lesicki
    series ordinal
    6
    0 references
    T Reinglass
    series ordinal
    7
    0 references
    T Varvil
    series ordinal
    8
    0 references
    B Otterud
    series ordinal
    9
    0 references
    M Leppert
    series ordinal
    10
    0 references
    publication date
    January 1995
    0 references
    volume
    56
    0 references
    issue
    1
    0 references
    page(s)
    188-92
    0 references
    cites work

    Identifiers

     
                      Retrieved from "https://www.wikidata.org/w/index.php?title=Q24672217&oldid=1475539149"