Latest revision | Your text |
| label / ast | label / ast |
| Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q
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| description / hy | description / hy |
| 1995 թվականի հունվարին հրատարակված գիտական հոդված
| | գիտական հոդված |
| description / sr | description / sr |
| научни чланак (објављен 1995-01)
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| description / ar | description / ar |
| مقالة علمية (نشرت عام 1995)
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| description / ko | description / ko |
| 1995년 논문
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| description / tg-cyrl | description / tg-cyrl |
| мақолаи илмӣ
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| description / ca | description / ca |
| article científic
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| description / bg | description / bg |
| научна статия
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| description / es | description / es |
| artículo científico publicado en 1995
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| description / lt | description / lt |
| mokslinis straipsnis
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| description / vi | description / vi |
| bài báo khoa học
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| description / ru | description / ru |
| научная статья
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| description / ast | description / ast |
| artículu científicu espublizáu en 1995
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| description / ka | description / ka |
| სამეცნიერო სტატია
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| description / zh-my | description / zh-my |
| 1995年论文
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| description / sq | description / sq |
| artikull shkencor
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| description / sr-ec | description / sr-ec |
| научни чланак
|
| description / he | description / he |
| מאמר מדעי
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| description / tg | description / tg |
| мақолаи илмӣ
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| description / nan | description / nan |
| 1995 nî lūn-bûn
|
| description / zh-hant | description / zh-hant |
| 1995年論文
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| description / sr-el | description / sr-el |
| naučni članak
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| description / eo | description / eo |
| scienca artikolo
|
| description / yue | description / yue |
| 1995年論文
|
| description / zh-hans | description / zh-hans |
| 1995年论文
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| description / nn | description / nn |
| vitskapeleg artikkel
|
| description / pt-br | description / pt-br |
| artigo científico (publicado na 1995)
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| description / hu | description / hu |
| tudományos cikk
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| description / zh-hk | description / zh-hk |
| 1995年論文
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| description / et | description / et |
| teaduslik artikkel
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| description / zh-tw | description / zh-tw |
| 1995年論文
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| description / oc | description / oc |
| article scientific
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| description / el | description / el |
| επιστημονικό άρθρο
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| description / tr | description / tr |
| bilimsel makale
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| description / zh-cn | description / zh-cn |
| 1995年论文
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| description / nb | description / nb |
| vitenskapelig artikkel
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| description / zh-mo | description / zh-mo |
| 1995年論文
|
| description / gl | description / gl |
| artigo científico
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| description / pl | description / pl |
| artykuł naukowy
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| description / th | description / th |
| บทความทางวิทยาศาสตร์
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| description / tl | description / tl |
| artikulong pang-agham
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| description / ro | description / ro |
| articol științific
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| description / zh-sg | description / zh-sg |
| 1995年论文
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| description / uk | description / uk |
| наукова стаття, опублікована в січні 1995
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| description / zh | description / zh |
| 1995年论文
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| description / ja | description / ja |
| 1995年の論文
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| description / wuu | description / wuu |
| 1995年论文
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| description / fi | description / fi |
| tieteellinen artikkeli
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| description / ur | description / ur |
| سائنسی مضمون
|
| description / fa | description / fa |
| مقالهٔ علمی
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| description / bn | description / bn |
| ১৯৯৫-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ
|
| description / hyw | description / hyw |
| 1995 թուականի Յունուարին հրատարակուած գիտական յօդուած
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| Property / PubMed publication ID | |
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| Property / PubMed publication ID: 7625443 / rank | |
| Deprecated rank
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| Property / PubMed publication ID: 7625443 / qualifier | |
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| Property / cites work: Strümpell's familial spastic paraplegia: genetics and neuropathology / reference |
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| Property / cites work: Strümpell's familial spastic paraplegia: genetics and neuropathology / reference | |
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| Property / cites work: The gene for Machado-Joseph disease maps to human chromosome 14q / reference |
| | | |
| Property / cites work: The gene for Machado-Joseph disease maps to human chromosome 14q / reference | |
| | |
| Property / cites work: Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q / reference |
| | | |
| Property / cites work: Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q / reference | |
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| Property / cites work | |
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| Property / cites work: Polymorphic DNA region adjacent to the 5' end of the human insulin gene / rank | |
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| Property / cites work: Polymorphic DNA region adjacent to the 5' end of the human insulin gene / reference | |
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| Property / cites work | |
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| Property / cites work: Multilocus linkage analysis in humans: detection of linkage and estimation of recombination / rank | |
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| Property / cites work: Multilocus linkage analysis in humans: detection of linkage and estimation of recombination / reference | |
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| Property / cites work | |
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| 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 | |
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| Property / cites work | |
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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. / 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 | |
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| Property / cites work | |
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| Property / cites work: Hereditary "pure" spastic paraplegia: a study of nine families / rank | |
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| Property / cites work: Hereditary "pure" spastic paraplegia: a study of nine families / reference | |
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| Property / cites work | |
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| 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 | |
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| Property / cites work | |
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| 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 | |
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| Property / cites work | |
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| Property / cites work: A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease). / rank | |
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| Property / cites work: A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease). / reference | |
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| Property / cites work | |
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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 / 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 | |
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| Property / cites work | |
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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 | |
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| Property / cites work | |
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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 | |
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| Property / cites work | |
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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 | |
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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 | |
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| Property / cites work | |
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| Property / cites work: HEREDITARY SPASTIC PARAPLEGIA. / rank | |
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| Property / cites work: HEREDITARY SPASTIC PARAPLEGIA. / reference | |
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| Property / cites work | |
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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 | |
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| Property / cites work | |
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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 | |
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| Property / cites work | |
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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 | |
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| Property / cites work | |
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| Property / cites work: DNA duplication associated with Charcot-Marie-Tooth disease type 1A / rank | |
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| Property / cites work: DNA duplication associated with Charcot-Marie-Tooth disease type 1A / reference | |
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| Property / cites work | |
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| Property / cites work: The phenotype of "pure" autosomal dominant spastic paraplegia / rank | |
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| Property / cites work: The phenotype of "pure" autosomal dominant spastic paraplegia / reference | |
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| Property / cites work | |
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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 | |
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| Property / cites work | |
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| Property / cites work: Sleep-associated breathing disorders in morbidly obese children and adolescents / rank | |
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| Property / cites work: Sleep-associated breathing disorders in morbidly obese children and adolescents / reference | |
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| Property / cites work: Sleep apnea, hypopnea and oxygen desaturation in normal subjects. A strong male predominance / rank | |
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| Property / cites work: Sleep apnea, hypopnea and oxygen desaturation in normal subjects. A strong male predominance / reference | |
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| Property / cites work: Medroxyprogesterone treatment of obstructive sleep apnea / rank | |
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| Property / cites work: Medroxyprogesterone treatment of obstructive sleep apnea / reference | |
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| Property / cites work: Sleep-disordered breathing and oxygen desaturation in obese patients / rank | |
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| Property / cites work: Sleep-disordered breathing and oxygen desaturation in obese patients / reference | |
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| Property / DOI | |
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| Property / DOI: 10.1002/AJMG.1320560215 / rank | |
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| Property / language of work or name: English / rank | |
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| Property / original language of film or TV show: English / rank |
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| Property / DOI |
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| Property / DOI: 10.1002/ajmg.1320560215 / rank |
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