英国将成立遗传数据咨询小组.

Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease.

Neuropathology and applied neurobiology·2006

Language barriers and paediatric burns: does education make a difference?

Burns : journal of the International Society for Burn Injuries·2006

Anatomical localization of leucine-rich repeat kinase 2 in mouse brain.

Neuroscience·2006

Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration.

Journal of medical genetics·2005

Progressive nonfluent aphasia and subsequent aphasic dementia associated with atypical progressive supranuclear palsy pathology.

European neurology·2003

Xeroderma pigmentosum/cockayne syndrome complex: first neuropathological study and review of eight other cases.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society·2002

Universal gates from braiding and fusing anyons on quantum hardware.

Nature·2026

People use fast and flat simulation to reason about new games.

Nature·2026

Rising dust pollution across Europe in a changing climate.

Nature·2026

Ammonia pressure controls colloidal metal nitride synthesis in molten salts.

Nature·2026

Programming fracture resistance in metamaterials via elastic instabilities.

Nature·2026

Selectivity Emerges from Indiscriminate Photoreduction.

Nature·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

相关实验视频

英国将成立遗传数据咨询小组.

相关概念视频

Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease.

Language barriers and paediatric burns: does education make a difference?

Anatomical localization of leucine-rich repeat kinase 2 in mouse brain.

Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration.

Progressive nonfluent aphasia and subsequent aphasic dementia associated with atypical progressive supranuclear palsy pathology.

Xeroderma pigmentosum/cockayne syndrome complex: first neuropathological study and review of eight other cases.

Universal gates from braiding and fusing anyons on quantum hardware.

People use fast and flat simulation to reason about new games.

Rising dust pollution across Europe in a changing climate.

Ammonia pressure controls colloidal metal nitride synthesis in molten salts.

Programming fracture resistance in metamaterials via elastic instabilities.

Selectivity Emerges from Indiscriminate Photoreduction.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

相关实验视频

英国将成立遗传数据咨询小组.

相关概念视频

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