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1. Screening Of Pathogenic Genes In Congenital Hypothyroidism With Thyroid Hypoplasia
2. Novel Pathological Mutation Screening For A Family Disorder Resembling Aarskog Syndrome
3. Disease Gene Mapping By The Application Of Next-generation Genomic Assays
4. Screening For The Causative Gene In An Autosomal Recessive Cerebellar Ataxia Pedigree Using Exome Sequencing
5. Effects Of Small Natural Compound On Lung Cancer Cells And Whole Genome Sequencing For Lung Cancer
6. Identification Of A Causative Gene In A High Myopia Family
7. Identification Of The Causative Genes For Three Families With Autosomal Dominant Hereditary Hearing Loss And One Family With Auditory Neuropathy
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