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Results: 1 to 13 of 13 (representing 11 labs)

Tests names and labsConditionsGenes and analytesMethods

Lactase deficiency, congenital

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

LCT. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

LCT. Detection of the mutation c.4170T>A (p.Tyr1390Ter) by sequencing

Instituto de Medicina Genomica
Spain
11
  • T Targeted variant analysis

LACTOSE INTOLERANCE - CONGENITAL LACTASE DEFICIENCY

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Congenital Lactase Deficiency , Sequencing LCT Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Congenital Diarrhea Seq + Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1821
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Diarrhea Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1821
  • D Deletion/duplication analysis

Congenital Diarrhea Seq Analysis

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1821
  • C Sequence analysis of the entire coding region

Abdominal Pain Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
6944
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital lactase deficiency

bio.logis Center for Human Genetics
Germany
11
  • T Targeted variant analysis

Lactase deficiency, congenital

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Congenital lactase deficiency (sequence analysis of LCT gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

LCT

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 13 of 13

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.

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