Products found: 16Search results

INTA University of Chile, Molecular Cytogenetic Laboratory

Disorder Genes Test Method Lab Info Product code  
INTA University of Chile, Molecular Cytogenetic Laboratory 22q11.2 Deletion Syndrome FISH-metaphase
INTA University of Chile, Molecular Cytogenetic Laboratory Angelman Syndrome UBE3A, FISH-metaphase
INTA University of Chile, Molecular Cytogenetic Laboratory Angelman Syndrome UBE3A, Methylation analysis
INTA University of Chile, Molecular Cytogenetic Laboratory Angelman Syndrome UBE3A, Sequence analysis of select exons
INTA University of Chile, Molecular Cytogenetic Laboratory Angelman Syndrome UBE3A, Uniparental disomy study (UPD)
INTA University of Chile, Molecular Cytogenetic Laboratory Charcot-Marie-Tooth Neuropathy Type 1A PMP22, Targeted mutation analysis
INTA University of Chile, Molecular Cytogenetic Laboratory FMR1-Related Disorders FMR1, Methylation analysis
INTA University of Chile, Molecular Cytogenetic Laboratory FMR1-Related Disorders FMR1, Targeted mutation analysis
INTA University of Chile, Molecular Cytogenetic Laboratory Hereditary Neuropathy with Liability to Pressure Palsies PMP22, Deletion/duplication analysis
INTA University of Chile, Molecular Cytogenetic Laboratory Prader-Willi Syndrome Deletion/duplication analysis
INTA University of Chile, Molecular Cytogenetic Laboratory Prader-Willi Syndrome FISH-interphase
INTA University of Chile, Molecular Cytogenetic Laboratory Prader-Willi Syndrome FISH-metaphase
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