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Results: 1 to 20 of 333

Tests names and labsConditionsGenes, analytes, and microbesMethods

Leukemia, acute myeloid, somatic, 601626 (Acute myeloid leukemia with recurrent genetic anomaly) V617F Mutation and (Exon 12-14) (JAK2 gene) (Dizi Analizi) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • E Sequence analysis of select exons

Leukemia, acute myeloid, somatic, 601626 (Acute myeloid leukemia) (PICALM gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, somatic, 601626 (Acute myeloid leukemia) (ETV6 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (KIT gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (CHIC2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (KRAS gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (NSD1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (LPP gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Unclassified acute myeloid leukemia) (CEBPA gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (NSD3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (RUNX1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (TERT gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, susceptibility to, 601626, Autosomal dominant (Unclassified acute myeloid leukemia) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Leukemia, acute myeloid, susceptibility to, 601626, Autosomal dominant (Unclassified acute myeloid leukemia) (GATA2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (SH3GL1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, somatic, 601626 (Unclassified acute myeloid leukemia) (FLT3 gene) (Sequence Analysis) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • E Sequence analysis of select exons

Leukemia, acute myeloid, somatic, 601626 (Acute myeloid leukemia) (NPM1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (MLF1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Leukemia, acute myeloid, 601626, Autosomal dominant (Acute myeloid leukemia) (MLLT10 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 333

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.