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Products found: 788Search results

Emory University School of Medicine, Emory Molecular Genetics Laboratory

Disorder Genes Test Method Lab Info Product code  
Emory University School of Medicine, Emory Molecular Genetics Laboratory Acid Sphingomyelinase Deficiency SMPD1, Sequence analysis of the entire coding region
Emory University School of Medicine, Emory Molecular Genetics Laboratory Acid Sphingomyelinase Deficiency SMPD1, Targeted mutation analysis
Emory University School of Medicine, Emory Molecular Genetics Laboratory ACTA1-Related Congenital Fiber-Type Disproportion ACTA1, Deletion/duplication analysis
Emory University School of Medicine, Emory Molecular Genetics Laboratory ACTA1-Related Congenital Fiber-Type Disproportion ACTA1, Sequence analysis of the entire coding region
Emory University School of Medicine, Emory Molecular Genetics Laboratory ACTA1-Related Nemaline Myopathy ACTA1, Deletion/duplication analysis
Emory University School of Medicine, Emory Molecular Genetics Laboratory ACTA1-Related Nemaline Myopathy ACTA1, Sequence analysis of the entire coding region
Emory University School of Medicine, Emory Molecular Genetics Laboratory Acyl-CoA Dehydrogenase 9 Deficiency ACAD9, Deletion/duplication analysis
Emory University School of Medicine, Emory Molecular Genetics Laboratory Acyl-CoA Dehydrogenase 9 Deficiency ACAD9, Sequence analysis of the entire coding region
Emory University School of Medicine, Emory Molecular Genetics Laboratory Adrenoleukodystrophy, X-Linked ABCD1, Deletion/duplication analysis
Emory University School of Medicine, Emory Molecular Genetics Laboratory Adrenoleukodystrophy, X-Linked ABCD1, Sequence analysis of the entire coding region
Emory University School of Medicine, Emory Molecular Genetics Laboratory Agenesis of the Corpus Callosum with Mental Retardation, Ocular Coloboma, and Micrognathia IGBP1, Deletion/duplication analysis
Emory University School of Medicine, Emory Molecular Genetics Laboratory Agenesis of the Corpus Callosum with Mental Retardation, Ocular Coloboma, and Micrognathia IGBP1, Sequence analysis of the entire coding region
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