• Home
  • Disorders
  • GeneReviews
  • Genes
  • Panels
  • Laboratories
  • Clinics
    • Select One: Disorders Genes Panels

Products found: 72Search results

University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik

Disorder Genes Test Method Lab Info Product code  
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik Achondroplasia FGFR3, Targeted mutation analysis
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik Alpha-B Crystallinopathy CRYAB, Sequence analysis of the entire coding region
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik Angelman Syndrome UBE3A, Methylation analysis
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik Angelman Syndrome UBE3A, Uniparental disomy study (UPD)
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik APC-Associated Polyposis Conditions APC, Deletion/duplication analysis
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik APC-Associated Polyposis Conditions APC, Mutation scanning of the entire coding region
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik APC-Associated Polyposis Conditions APC, Sequence analysis of the entire coding region
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik Atypical Werner Syndrome LMNA, Linkage analysis
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik Atypical Werner Syndrome LMNA, Sequence analysis of the entire coding region
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik BMPR1A-Related Juvenile Polyposis BMPR1A, Deletion/duplication analysis
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik BMPR1A-Related Juvenile Polyposis BMPR1A, Sequence analysis of the entire coding region
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik CFTR-Related Disorders CFTR, Sequence analysis of select exons
Loading...