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Results: 1 to 11 of 11

Tests names and labsConditionsGenes, analytes, and microbesMethods

SYT2

MGZ Medical Genetics Center
Germany
11
  • S Mutation scanning of the entire coding region

Newborn: Neonatal Apneas

MGZ Medical Genetics Center
Germany
213
  • C Sequence analysis of the entire coding region

Congenital Myasthenic Syndrome (CMS)

MGZ Medical Genetics Center
Germany
117
  • C Sequence analysis of the entire coding region

Congenital myasthenic syndrome ALG14-related

MGZ Medical Genetics Center
Germany
11
  • C Sequence analysis of the entire coding region

CHRNB1-Related Congenital Myasthenic Syndrome

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

CHRNA1-Related Congenital Myasthenic Syndrome

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

RAPSN-Related Congenital Myasthenic Syndrome

MGZ Medical Genetics Center
Germany
21
  • E Sequence analysis of select exons

CHRND-Related Congenital Myasthenic Syndrome

MGZ Medical Genetics Center
Germany
31
  • C Sequence analysis of the entire coding region

CHRNE-Related Congenital Myasthenic Syndrome

MGZ Medical Genetics Center
Germany
41
  • C Sequence analysis of the entire coding region

DOK7-Related Congenital Myasthenic Syndrome

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

AGRN-Related Congenital Myasthenic Syndrome

MGZ Medical Genetics Center
Germany
21
  • E Sequence analysis of select exons

Results: 1 to 11 of 11

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.