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Products found: 382Search results

Instituto de Medicina Genmica, IMEGEN

Disorder Genes Test Method Lab Info Product code  
Instituto de Medicina Genómica, IMEGEN 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP21A2, Deletion/duplication analysis
Instituto de Medicina Genómica, IMEGEN 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP21A2, Targeted mutation analysis
Instituto de Medicina Genómica, IMEGEN 22q11.2 Deletion Syndrome Deletion/duplication analysis
Instituto de Medicina Genómica, IMEGEN 22q11.2 Deletion Syndrome Linkage analysis
Instituto de Medicina Genómica, IMEGEN 46,XX Testicular Disorder of Sex Development SRY, Deletion/duplication analysis
Instituto de Medicina Genómica, IMEGEN 46,XX Testicular Disorder of Sex Development SRY, Sequence analysis of the entire coding region
Instituto de Medicina Genómica, IMEGEN Achondroplasia FGFR3, Sequence analysis of the entire coding region
Instituto de Medicina Genómica, IMEGEN Achondroplasia FGFR3, Targeted mutation analysis
Instituto de Medicina Genómica, IMEGEN Acute Intermittent Porphyria HMBS, Sequence analysis of the entire coding region
Instituto de Medicina Genómica, IMEGEN ACVRL1-Related Hereditary Hemorrhagic Telangiectasia ACVRL1, Sequence analysis of the entire coding region
Instituto de Medicina Genómica, IMEGEN Adrenoleukodystrophy, X-Linked ABCD1, Sequence analysis of the entire coding region
Instituto de Medicina Genómica, IMEGEN ALG6-CDG (CDG-Ic) ALG6, Sequence analysis of the entire coding region
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