Article - Cell Press
Từ khóa » C.1a G
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NM_000152.5(GAA):c.1A>G (p.Met1Val) AND Glycogen ... - NCBI
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ClinVar Genomic Variation As It Relates To Human Health - NCBI
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Germline C.1A>C Heterozygous Pathogenic Variant In SDHA ...
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Lynch Syndrome Mutation Spectrum In New South Wales, Australia ...
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Compound Heterozygosity For Two MSH2 Mutations Suggests Mild ...
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Submissions For Variant NM_000251.3(MSH2):c.1A>G (p.Met1Val ...
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Submissions For Variant NM_000535.7(PMS2):c.1A>G (p.Met1Val ...
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The PHF6 Mutation C.1A>G; PM1V Causes Börjeson-Forsman ...
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Mutation Details For C.1A>G - Cystic Fibrosis Mutation Database
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Mutation Overview Page HIST1H4L - P.M1_?4 ( Frameshift) - COSMIC
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Epidermolysis Bullosa Simplex Due To KLHL24 (c.1A>G, P.1Met ...
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Clinical Genome Resources - Evidence Repository
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A New Variant (c.1A>G) In LDLRAP1 Causing Autosomal Recessive ...