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journal of human genetics
  
سال:2015 - دوره:60 - شماره:7
  
 
A commentary on short-term efficacy of N -carbamylglutamate in a patient with N -acetylglutamate synthase deficiency
- صفحه:347-347
  
 
A dual origin of Tibetans: evidence from mitochondrial genomes
- صفحه:403-404
  
 
A novel mutation in the promoter of RARS2 causes pontocerebellar hypoplasia in two siblings
- صفحه:363-369
  
 
Associations between the polymorphisms of GSTT1, GSTM1 and methylation of arsenic in the residents exposed to low-level arsenic in drinking water in China
- صفحه:387-394
  
 
Biotin-responsive basal ganglia disease: a case diagnosed by whole exome sequencing
- صفحه:381-385
  
 
Fine mapping and resequencing of the PARK16 locus in Parkinson’s disease
- صفحه:357-362
  
 
Genetic and linguistic correlation of the Kra–Dai-speaking groups in Thailand
- صفحه:371-380
  
 
Patterns and functional roles of LINE-1 and Alu methylation in the keratinocyte from patients with psoriasis vulgaris
- صفحه:349-355
  
 
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia
- صفحه:399-401
  
 
Short-term efficacy of N -carbamylglutamate in a patient with N -acetylglutamate synthase deficiency
- صفحه:395-397
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