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Results: 81 to 91 of 91

Tests names and labsConditionsGenes, analytes, and microbesMethods

Spinal Muscular Atrophy Panel

CeGaT GmbH
Germany
1127
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel

CeGaT GmbH
Germany
147143
  • C Sequence analysis of the entire coding region

Neuropathy

MGZ Medical Genetics Center
Germany
7122
  • C Sequence analysis of the entire coding region

Muscle Weakness Manifesting in Adulthood / Limb-Girdle Muscular Dystrophy (AD and AR)

MGZ Medical Genetics Center
Germany
690
  • C Sequence analysis of the entire coding region

Muscle Weakness (Myopathy, Muscular Dystrophy)

MGZ Medical Genetics Center
Germany
6179
  • C Sequence analysis of the entire coding region

Muscle Disease with Distal Myopathy

MGZ Medical Genetics Center
Germany
628
  • C Sequence analysis of the entire coding region

Spinal Muscular Atrophy, Proximal Motor Neuropathy

MGZ Medical Genetics Center
Germany
314
  • C Sequence analysis of the entire coding region

Newborn: “Floppy Infant “

MGZ Medical Genetics Center
Germany
673
  • C Sequence analysis of the entire coding region

Amyotrophic Lateral Sclerosis (ALS) and Phenocopies

MGZ Medical Genetics Center
Germany
223
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BICD2

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

Results: 81 to 91 of 91

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.