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| (30 intermediate revisions by 12 users not shown) |
| label / nl | label / nl |
| | | Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q |
| label / ast | label / ast |
| | | Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q |
| description / sv | description / sv |
| | | vetenskaplig artikel (publicerad på 1995-01) |
| description / da | description / da |
| | | videnskabelig artikel (udgivet 1995-01) |
| description / it | description / it |
| | | articolo scientifico (pubblicato il 1995-01) |
| description / sk | description / sk |
| | | vedecký článok (publikovaný 1995-01) |
| description / pt | description / pt |
| | | artigo científico (publicado na 1995-01) |
| description / hy | description / hy |
| | | 1995 թվականի հունվարին հրատարակված գիտական հոդված |
| description / sr | description / sr |
| | | научни чланак (објављен 1995-01) |
| description / ar | description / ar |
| | | مقالة علمية (نشرت عام 1995) |
| description / ko | description / ko |
| | | 1995년 논문 |
| description / tg-cyrl | description / tg-cyrl |
| | | мақолаи илмӣ |
| description / ca | description / ca |
| | | article científic |
| description / bg | description / bg |
| | | научна статия |
| description / es | description / es |
| | | artículo científico publicado en 1995 |
| description / lt | description / lt |
| | | mokslinis straipsnis |
| description / vi | description / vi |
| | | bài báo khoa học |
| description / ru | description / ru |
| | | научная статья |
| description / ast | description / ast |
| | | artículu científicu espublizáu en 1995 |
| description / ka | description / ka |
| | | სამეცნიერო სტატია |
| description / zh-my | description / zh-my |
| | | 1995年论文 |
| description / sq | description / sq |
| | | artikull shkencor |
| description / sr-ec | description / sr-ec |
| | | научни чланак |
| description / he | description / he |
| | | מאמר מדעי |
| description / tg | description / tg |
| | | мақолаи илмӣ |
| description / nan | description / nan |
| | | 1995 nî lūn-bûn |
| description / zh-hant | description / zh-hant |
| | | 1995年論文 |
| description / sr-el | description / sr-el |
| | | naučni članak |
| description / eo | description / eo |
| | | scienca artikolo |
| description / yue | description / yue |
| | | 1995年論文 |
| description / zh-hans | description / zh-hans |
| | | 1995年论文 |
| description / nn | description / nn |
| | | vitskapeleg artikkel |
| description / pt-br | description / pt-br |
| | | artigo científico (publicado na 1995) |
| description / hu | description / hu |
| | | tudományos cikk |
| description / zh-hk | description / zh-hk |
| | | 1995年論文 |
| description / et | description / et |
| | | teaduslik artikkel |
| description / zh-tw | description / zh-tw |
| | | 1995年論文 |
| description / oc | description / oc |
| | | article scientific |
| description / el | description / el |
| | | επιστημονικό άρθρο |
| description / tr | description / tr |
| | | bilimsel makale |
| description / zh-cn | description / zh-cn |
| | | 1995年论文 |
| description / nb | description / nb |
| | | vitenskapelig artikkel |
| description / zh-mo | description / zh-mo |
| | | 1995年論文 |
| description / gl | description / gl |
| | | artigo científico |
| description / pl | description / pl |
| | | artykuł naukowy |
| description / th | description / th |
| | | บทความทางวิทยาศาสตร์ |
| description / tl | description / tl |
| | | artikulong pang-agham |
| description / ro | description / ro |
| | | articol științific |
| description / zh-sg | description / zh-sg |
| | | 1995年论文 |
| description / uk | description / uk |
| | | наукова стаття, опублікована в січні 1995 |
| description / zh | description / zh |
| | | 1995年论文 |
| description / ja | description / ja |
| | | 1995年の論文 |
| description / wuu | description / wuu |
| | | 1995年论文 |
| description / fi | description / fi |
| | | tieteellinen artikkeli |
| description / ur | description / ur |
| | | سائنسی مضمون |
| description / fa | description / fa |
| | | مقالهٔ علمی |
| description / bn | description / bn |
| | | ১৯৯৫-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ |
| description / hyw | description / hyw |
| | | 1995 թուականի Յունուարին հրատարակուած գիտական յօդուած |
| Property / original language of film or TV show | |
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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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| 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 / PubMed publication ID |
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| Property / PubMed publication ID: 7625443 / rank |
| | | Deprecated rank |
| Property / PubMed publication ID: 7625443 / qualifier |
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| Property / cites work |
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| Property / cites work: The gene for Machado-Joseph disease maps to human chromosome 14q / rank |
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| Property / cites work: The gene for Machado-Joseph disease maps to human chromosome 14q / reference |
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| Property / cites work: Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q / rank |
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| 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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 |
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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: 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: 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: 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: 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: 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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