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- 2014
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Mark
Comprehensive genetic characterization of pediatric T-cell acute lymphoblastic leukemia
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- Contribution to journal › Published meeting abstract
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Mark
Neuroacanthocytosis - Clinical variability (a report on six cases)
2014) Eighteenth International Congress of Parkinson's Disease and Movement Disorders In Movement Disorders 29(Suppl 1). p.194-194(
- Contribution to journal › Published meeting abstract
- 2013
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Mark
Heterozygous FA2H mutations in autism spectrum disorders
(
- Contribution to journal › Article
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Mark
ACAC beta gene (rs2268388) and AGTR1 gene (rs5186) polymorphism and the risk of nephropathy in Asian Indian patients with type 2 diabetes
(
- Contribution to journal › Article
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Mark
Microphthalmia transcription factor regulates pancreatic β-cell function
(
- Contribution to journal › Article
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Mark
EpiHealth: a large population-based cohort study for investigation of gene-lifestyle interactions in the pathogenesis of common diseases
(
- Contribution to journal › Article
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Mark
Functional Mannose-Binding Lectin Haplotype Variants are Associated with Alzheimer's Disease
(
- Contribution to journal › Article
- 2012
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Mark
The global distribution and evolution of deoxyribonucleoside kinases in bacteria
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- Contribution to journal › Article
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Mark
Myeloid malignancies with acquired trisomy 21 as the sole cytogenetic change are clinically highly variable and display a heterogeneous pattern of copy number alterations and mutations(a).
(
- Contribution to journal › Article
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Mark
Friedreich's ataxia in patients with FXN p.R165P point mutation
2012) 16th Congress of the European-Federation-of-Neurological-Societies (EFNS) In European Journal of Neurology 19(Suppl 1). p.727-727(
- Contribution to journal › Published meeting abstract