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Sanger Validation Results Of Identified Ca2 Gene Variant C 368g A

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A Sanger Validation Of Nm_001252.5:c.332c>t Mutation. B Krec Copy ...
Sanger Validation Of Final Modifier Gene Candidate Variants. All Nine ...
Sanger Sequencing Confirmed The Variant Of C.2696c > G (p.ala899gly) In ...
Sanger Sequencing Validation Of The N309k Variant. Sanger Sequencing Of ...
The Sanger Sequencing And Conservation Analysis Of The Novel Variant ...

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Sanger sequence analysis for validation of exome sequencing variant ... — Sanger sequence analysis for validation of exome sequencing ...

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Sanger sequence analysis for validation of exome sequencing variant ... — Sanger sequence analysis for validation of exome sequencing ...

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Sanger validation of the variants, conservation and splice analysis. a ... — Sanger validation of the variants, conservation and splice a...

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Sanger sequencing for variant validation and segregation analyses. In ... — Sanger sequencing for variant validation and segregation ana...

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The Sanger sequencing and conservation analysis of the novel variant ... — The Sanger sequencing and conservation analysis of the novel...

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Sanger validation and segregation analysis of VARS1 variant identified ... — Sanger validation and segregation analysis of VARS1 variant ...

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Sanger sequencing confirmed the variant of c.2696C > G (p.Ala899Gly) in ... — Sanger sequencing confirmed the variant of c.2696C > G (p.Al...

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| Sanger sequencing results of the three variants identified. (A-C ... — | Sanger sequencing results of the three variants identified...

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Sanger sequencing results of homozygous c.1642C>T pathogenic variant ... — Sanger sequencing results of homozygous c.1642C>T pathogenic...

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Sanger validation of the breakpoints. a Sanger sequence of proband ... — Sanger validation of the breakpoints. a Sanger sequence of p...

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Sanger sequencing validation of variants identified by whole-exome ... — Sanger sequencing validation of variants identified by whole...

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Sanger validation of final modifier gene candidate variants. All nine ... — Sanger validation of final modifier gene candidate variants....

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Sanger sequencing electropherogram. The variant (c.389A > G ... — Sanger sequencing electropherogram. The variant (c.389A > G ...

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Sanger sequencing for variant validation and segregation analyses. In ... — Sanger sequencing for variant validation and segregation ana...

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Characteristics of the GPR84 variant. (A) Sanger sequencing validation ... — Characteristics of the GPR84 variant. (A) Sanger sequencing ...

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Sanger sequencing validation results of the pathogenic mutation of the ... — Sanger sequencing validation results of the pathogenic mutat...

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Sanger sequencing electropherogram. The variant (c.389A > G ... — Sanger sequencing electropherogram. The variant (c.389A > G ...

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Sanger sequencing data of (A-C) the three novel variants identified in ... — Sanger sequencing data of (A-C) the three novel variants ide...

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Sanger sequencing results of the three variants identified. (A–C ... — Sanger sequencing results of the three variants identified. ...

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| (A) Sanger sequencing validation of the variant c.1918G>T in the ... — | (A) Sanger sequencing validation of the variant c.1918G>T ...

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Sanger sequencing validation of variants identified by whole-exome ... — Sanger sequencing validation of variants identified by whole...

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(A) Patient 1 carried the variant of c.1803C > G, the results of sanger ... — (A) Patient 1 carried the variant of c.1803C > G, the result...

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Variants evaluated by Sanger sequencing. Gene, variant location, effect ... — Variants evaluated by Sanger sequencing. Gene, variant locat...

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| Validation via Sanger sequencing. The G>T variant identified in three ... — | Validation via Sanger sequencing. The G>T variant identifi...

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Sanger validation results of identified CA2 gene variant (c.368G > A ... — Sanger validation results of identified CA2 gene variant (c....

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Variant validation using Sanger sequencing and realtime PCR. (A) Minor ... — Variant validation using Sanger sequencing and realtime PCR....

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Sanger validation of final modifier gene candidate variants. All nine ... — Sanger validation of final modifier gene candidate variants....

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a Sanger validation of NM_001252.5:c.332C>T mutation. b KREC copy ... — a Sanger validation of NM_001252.5:c.332C>T mutation. b KREC...

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Sanger sequencing validation of the N309K variant. Sanger sequencing of ... — Sanger sequencing validation of the N309K variant. Sanger se...

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Sanger sequencing of a family with CASK gene c.764G > A missense ... — Sanger sequencing of a family with CASK gene c.764G > A miss...

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CDC42 c.68A>G variant validation through Sanger sequencing. A ... — CDC42 c.68A>G variant validation through Sanger sequencing. ...

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Sanger sequencing validation of the de novo variants identified by ... — Sanger sequencing validation of the de novo variants identif...

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Validation and gene dosage effect of variants in CLCNKB. (a) Sanger ... — Validation and gene dosage effect of variants in CLCNKB. (a)...

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Sanger sequencing results of homozygous c.1642C>T pathogenic variant ... — Sanger sequencing results of homozygous c.1642C>T pathogenic...

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Sanger sequencing chromatograms of the variant c.1183 + 1 G > C from ... — Sanger sequencing chromatograms of the variant c.1183 + 1 G ...

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