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Results: 21 to 30 of 30

Tests names and labsConditionsGenes, analytes, and microbesMethods

MARSHALL-SMITH SYNDROME

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

Marshall-Smith Syndrome , Sequencing NFIX Gene

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

Invitae Overgrowth and Macrocephaly Syndromes Panel

Invitae
United States
4320
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NFIX Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Marshall-Smith syndrome

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

Single gene testing NFIX

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Sotos Syndrom 2 (NFIX)

MVZ Dr. Eberhard & Partner Dortmund
Germany
21
  • C Sequence analysis of the entire coding region

NFIX Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NFIX

MGZ Medical Genetics Center
Germany
21
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 30 of 30

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.