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High-throughput single nucleotide polymorphism genotyping in wheat (Triticum spp.).
Genotyping technologies for genetic research.
Involvement of hypertrophic cardiomyopathy genes in sudden infant death syndrome (SID)
The -9247 T/C polymorphism in the SOST upstream regulatory region that potentially affects C/EBPalpha and FOXA1 binding is associated with osteoporosis.
Development and evaluation of a PCR and mass spectroscopy (PCR-MS)-based method for quantitative, type-specific detection of human papillomavirus.
GATA-2 L359 V mutation is exclusively associated with CML progression but not other hematological malignancies and GATA-2 P250A is a novel single nucleotide polymorphism.
Genomewide association studies of stroke.
Genetic Risk Prediction – Are we there yet?
Genetics of type 1A diabetes.
Reduced Neutrophil Count in People of African Descent Is Due To a Regulatory Variant in the Duffy Antigen Receptor for Chemokines Gene
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